CN115335383A

CN115335383A - Cyclic compound for organic electroluminescent device

Info

Publication number: CN115335383A
Application number: CN202180024276.1A
Authority: CN
Inventors: 菲利普·斯托塞尔
Original assignee: Merck Patent GmbH
Current assignee: Merck Patent GmbH
Priority date: 2020-03-26
Filing date: 2021-03-23
Publication date: 2022-11-11
Also published as: KR20220158771A; US20230157171A1; EP4126880A1; WO2021191183A1

Abstract

The present invention relates to cyclic compounds suitable for use in electronic devices, and to electronic devices, in particular organic electroluminescent devices, containing said compounds.

Description

Cyclic compound for organic electroluminescent device

The present invention relates to cyclic compounds for use in electronic devices, in particular in organic electroluminescent devices, and to electronic devices, in particular organic electroluminescent devices, comprising these heterocyclic compounds.

The light emitting material used in the organic electroluminescent device is generally a phosphorescent organometallic complex or a fluorescent compound. There is still a general need for improved electroluminescent devices.

WO 2010/104047 A1 and WO 2019/132506 A1 disclose polycyclic compounds useful for organic electroluminescent devices. No compounds according to the invention are disclosed. Furthermore, wang et al, nature Commission | 8. However, wang et al do not describe the use of these compounds in organic electroluminescent devices.

In general, there is still a need for improvements in the heterocyclic compounds, for example for use as emitters, in particular as fluorescent emitters, in particular with regard to the lifetime and color purity of the devices, but also with regard to the efficiency and operating voltage of the devices.

It is therefore an object of the present invention to provide compounds which are suitable for use in organic electronic devices, especially organic electroluminescent devices, and which lead to good device properties when used in such devices; and to provide a corresponding electronic device.

More particularly, the problem addressed by the present invention is to provide compounds that result in long life, good efficiency and low operating voltage.

Furthermore, the compounds should have excellent processability and the compounds should in particular show good solubility.

Another problem solved by the present invention may be considered to be to provide compounds suitable for use in phosphorescent or fluorescent electroluminescent devices, in particular as emitters. More particularly, the problem addressed by the present invention is to provide a light emitter suitable for red, green or blue electroluminescent devices.

Furthermore, the compounds, especially when they are used as emitters in organic electroluminescent devices, should lead to devices having excellent color purity.

Another problem solved by the present invention may be considered to be to provide compounds suitable for use in phosphorescent or fluorescent electroluminescent devices, in particular as matrix materials. More particularly, the problem addressed by the present invention is to provide matrix materials suitable for red, yellow and blue phosphorescent electroluminescent devices.

Furthermore, the compounds, especially when they are used as matrix materials, as hole transport materials or as electron transport materials in organic electroluminescent devices, lead to devices with excellent color purity.

Another problem that can be considered is to provide electronic devices with excellent performance at a very low price and with a stable quality.

Furthermore, it should be possible to use or adapt the electronic device for many purposes. More particularly, the performance of the electronic device should be maintained over a wide temperature range.

Surprisingly, it has been found that this object is achieved by specific compounds which are described in detail below, which are very suitable, preferably for use in electroluminescent devices, and which lead to organic electroluminescent devices exhibiting very good properties, in particular with respect to lifetime, color purity, efficiency and operating voltage. The present invention therefore provides these compounds and electronic devices, especially organic electroluminescent devices, comprising such compounds.

The present invention provides a compound comprising at least one structure of formula (I), preferably a compound of formula (I),

the symbols and subscripts used therein are as follows:

Z ¹ 、Z ² in each case identical or different and is N or B;

W ¹ 、W ² 、W ³ 、W ⁴ in each case identical or different, and is either CAr, X, or two adjacent W ¹ 、W ² 、W ³ 、W ⁴ The group is Ar;

Y ¹ in each case identical or different and are N (Ar), N (R), P (A)r)、P(R)、P(＝O)Ar、P(＝O)R、P(＝S)Ar、P(＝S)R、B(Ar)、B(R)、Al(Ar)、Al(R)、Ga(Ar)、Ga(R)、C＝O、C(R) ₂ 、Si(R) ₂ 、C＝NR、C＝NAr、C＝C(R) ₂ O, S, se, S = O or SO ₂ N (Ar), N (R), B (Ar), B (R), P (= O) R, P (= O) Ar, C = O, C (R) are preferable ₂ 、Si(R) ₂ O, S, se, S = O or SO ₂ More preferably C = O, N (Ar) or B (Ar);

Y ² identical or different in each case and is a bond, N (Ar), N (R), P (Ar), P (R), P (= O) Ar, P (= O) R, P (= S) Ar, P (= S) R, B (Ar), B (R), al (Ar), al (R), ga (Ar), ga (R), C = O, C (R) ₂ 、Si(R) ₂ 、C＝NR、C＝NAr、C＝C(R) ₂ O, S, se, S = O or SO ₂ Preferred are a bond, N (Ar), N (R), B (Ar), B (R), P (= O) R, P (= O) Ar, C = O, C (R) ₂ 、Si(R) ₂ O, S, se, S = O or SO ₂ More preferably C = O, N (Ar) or B (Ar);

ar is identical or different on each occurrence and is an aromatic or heteroaromatic ring system having from 5 to 60 aromatic ring atoms and which may be substituted by one or more R groups; here, the Ar group may form a ring system with at least one Ar group, R group or further group;

x is identical or different on each occurrence and is N or CR, preferably CR, with the proviso that in one ring X, X ³ No more than two of the groups are N;

X ¹ in each case the same or different, and is N, CR ^a Or CAr, preferably CR ^a Provided that X is in a ring ¹ 、X ² 、X ³ No more than two of the groups are N;

X ² in each case the same or different, and is N, CR ^b Or CAr, preferably CR ^b Provided that X is in a ring ¹ 、X ² 、X ³ No more than two of the groups are N;

X ³ in each case the same or different, and is N, CR ^c CAr, or X if p is 1 ³ Is a compound of the formula (I) C,preferably X ³ Is CR ^c Provided that in a ring X, X ¹ 、X ² 、X ³ No more than two of the groups are N;

p is identical or different and is 0 or 1, where if W ³ 、W ⁴ Not Ar, p =1;

R、R ^a 、R ^b 、R ^c in each case identical or different and are H, D, OH, F, cl, br, I, CN, NO ₂ ，N(Ar') ₂ ，N(R ¹ ) ₂ ，C(＝O)OAr'，C(＝O)OR ¹ ，C(＝O)N(Ar') ₂ ，C(＝O)N(R ¹ ) ₂ ，C(Ar') ₃ ，C(R ¹ ) ₃ ，Si(Ar') ₃ ，Si(R ¹ ) ₃ ，B(Ar') ₂ ，B(R ¹ ) ₂ ，C(＝O)Ar'，C(＝O)R ¹ ，P(＝O)(Ar') ₂ ，P(＝O)(R ¹ ) ₂ ，P(Ar') ₂ ，P(R ¹ ) ₂ ，S(＝O)Ar'，S(＝O)R ¹ ，S(＝O) ₂ Ar'，S(＝O) ₂ R ¹ ，OSO ₂ Ar'，OSO ₂ R ¹ Straight-chain alkyl, alkoxy or thioalkoxy groups having from 1 to 40 carbon atoms or alkenyl or alkynyl groups having from 2 to 40 carbon atoms or branched or cyclic alkyl, alkoxy or thioalkoxy groups having from 3 to 20 carbon atoms, where the alkyl, alkoxy, thioalkoxy, alkenyl or alkynyl groups can in each case be substituted by one or more R ¹ Substituted by radicals in which one or more non-adjacent CH ₂ The group can be represented by R ¹ C＝CR ¹ 、C≡C、Si(R ¹ ) ₂ 、C＝O、C＝S、C＝Se、C＝NR ¹ 、-C(＝O)O-、-C(＝O)NR ¹ -、NR ¹ 、P(＝O)(R ¹ ) -O-, -S-, SO or SO ₂ Instead of, or with 5 to 60 aromatic ring atoms and can be substituted in each case by one or more R ¹ Aromatic or heteroaromatic ring systems substituted by radicals, or having 5 to 60 aromatic ring atoms and which may be substituted by one or more R ¹ A group-substituted aryloxy or heteroaryloxy group; simultaneously, two R, R ^a 、R ^b 、R ^c The radicals may also form a ring system together or with further radicals;

ar' is identical or different on each occurrence and is an aromatic ring having 5 to 60 aromatic ring atoms and may be substituted by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system; also, the two Ar' groups bonded to the same carbon, silicon, nitrogen, phosphorus or boron atom may be further linked via a bridging group by a single bond or selected from B (R) ¹ )、C(R ¹ ) ₂ 、Si(R ¹ ) ₂ 、C＝O、C＝NR ¹ 、C＝C(R ¹ ) ₂ 、O、S、S＝O、SO ₂ 、N(R ¹ )、P(R ¹ ) And P (= O) R ¹ Are linked together;

R ¹ in each case identical or different and are H, D, F, cl, br, I, CN, NO ₂ ，N(Ar″) ₂ ，N(R ² ) ₂ ，C(＝O)OAr″，C(＝O)OR ² ，C(＝O)Ar″，C(＝O)R ² ，P(＝O)(Ar″) ₂ ，P(Ar″) ₂ ，B(Ar″) ₂ ，B(R ² ) ₂ ，C(Ar″) ₃ ，C(R ² ) ₃ ，Si(Ar″) ₃ ，Si(R ² ) ₃ A linear alkyl, alkoxy or thioalkoxy group having from 1 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having from 3 to 40 carbon atoms or an alkenyl group having from 2 to 40 carbon atoms, each of which may be substituted by one or more R ² Radical substitution of one or more non-adjacent CH ₂ The group may be represented by-R ² C＝CR ² -、-C≡C-、Si(R ² ) ₂ 、C＝O、C＝S、C＝Se、C＝NR ² 、-C(＝O)O-、-C(＝O)NR ² -、NR ² 、P(＝O)(R ² ) -O-, -S-, SO or SO ₂ And wherein one or more hydrogen atoms may be replaced by D, F, cl, br, I, CN or NO ₂ Instead of, or as aromatic or heteroaromatic ring systems having from 5 to 60 aromatic ring atoms, each of which may be substituted by one or more R ² Substituted by radicals, or having 5 to 60 aromatic ring atoms and being able to be substituted by one or morePlural R ² Aryloxy or heteroaryloxy radicals substituted by radicals, or having 5 to 60 aromatic ring atoms and which may be substituted by one or more R ² A group-substituted aralkyl or heteroaralkyl group, or a combination of these systems; simultaneously, two or more preferably adjacent R ¹ The groups may together form a ring system; at the same time, one or more R ¹ A group may form a ring system with another part of the compound;

ar' is identical or different on each occurrence and is a cyclic aromatic compound having from 5 to 30 aromatic ring atoms and which may be substituted by one or more R ² A group-substituted aromatic or heteroaromatic ring system; at the same time, the two Ar' groups bonded to the same carbon, silicon, nitrogen, phosphorus or boron atom may also be linked via a bridging group by a single bond or be selected from B (R) ² )、C(R ² ) ₂ 、Si(R ² ) ₂ 、C＝O、C＝NR ² 、C＝C(R ² ) ₂ 、O、S、S＝O、SO ₂ 、N(R ² )、P(R ² ) And P (= O) R ² Are linked together;

R ² identical or different on each occurrence and selected from H, D, F, CN, an aliphatic hydrocarbon radical having from 1 to 20 carbon atoms or an aromatic or heteroaromatic ring system having from 5 to 30 aromatic ring atoms in which one or more hydrogen atoms may be replaced by D, F, cl, br, I or CN and which may be substituted by one or more alkyl radicals each having from 1 to 4 carbon atoms; simultaneously, two or more preferably adjacent substituents R ² May together form a ring system.

In formula (I), p may be the same or different and may be 0 or 1, wherein if W is ³ 、W ⁴ Not Ar, then p =1. Therefore, if W ³ 、W ⁴ Together form an aromatic or heteroaromatic ring system having from 5 to 60 aromatic ring atoms and which may be substituted by one or more R groups, then p may be only 0. If p =0, then W is added ³ 、W ⁴ An aromatic or heteroaromatic ring system which is formed by a group and can be substituted by an R group and Z in the formula (I) ² The groups are combined. In addition, if p =1, then W ³ 、W ⁴ The group may be Ar. In this case, W ³ 、W ⁴ The radicals together form an aromatic or heteroaromatic ring system having from 5 to 60 aromatic ring atoms and which may be substituted by one or more R groups, wherein the aromatic or heteroaromatic ring system is bonded to Z via two adjacent carbon atoms of the formula (I) which are bonded to one another ² And Y ² The group being bound to Z ² And Y ² The groups together form a six-membered ring. If W ¹ 、W ² The group is Ar, the aromatic or heteroaromatic ring system is bonded to Z via two adjacent carbon atoms of the formula (I) ¹ And Y ¹ The group being bound to Z ¹ And Y ¹ The groups together form a six-membered ring.

This is explained in detail below by the formulae (Ia), (Ib), (Ic) and (Id). Here, formulae (Ia) and (Ib) show the case where p =1 and formula (Ic) shows the case where p =0, which are detailed above. If W is ¹ 、W ² When the radicals together are Ar, formula (Id) applies accordingly.

In formula (I), p may be the same or different, and may be 0 or 1, wherein:

-when p =1, formula (I) complies with formula (Ia) or (Ib);

-when p =0, formula (I) complies with formula (Ic):

in the formula (I), W ¹ 、W ² The groups together may be Ar. This gives the formula (Id):

in formulae (Ia), (Ib), (Ic) and (Id), the symbols have the definitions detailed above for formula (I).

In the context of the present invention, an aryl group contains from 6 to 40 carbon atoms; in the context of the present invention, a heteroaryl group contains from 2 to 40 carbon atoms and at least one heteroatom, with the proviso that the sum of carbon atoms and heteroatoms is at least 5. The heteroatoms are preferably selected from N, O and/or S. Here, an aryl group or heteroaryl group is understood to mean a simple aromatic ring, i.e. benzene, or a simple heteroaromatic ring, such as pyridine, pyrimidine, thiophene, etc., or a fused (annellated) aryl or heteroaryl group, such as naphthalene, anthracene, phenanthrene, quinoline, isoquinoline, etc. In contrast, aromatic compounds, such as biphenyl, which are connected to one another by single bonds, are not referred to as aryl or heteroaryl groups, but rather as aromatic ring systems.

In the context of the present invention, an electron-deficient heteroaryl group is a heteroaryl group having at least one heteroaromatic six-membered ring containing at least one nitrogen atom. Additional aromatic or heteroaromatic five-or six-membered rings may be fused to the six-membered ring. Examples of electron-deficient heteroaryl groups are pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinoline, quinazoline or quinazoline

And (3) an alkyl group.

In the context of the present invention, an aromatic ring system contains from 6 to 60 carbon atoms in the ring system. In the context of the present invention, a heteroaromatic ring system contains from 2 to 60 carbon atoms and at least one heteroatom in the ring system, with the proviso that the sum of carbon atoms and heteroatoms is at least 5. The heteroatoms are preferably selected from N, O and/or S. In the context of the present invention, aromatic or heteroaromatic ring systems are understood as meaning the following systems: it need not contain only aryl or heteroaryl groups, but wherein two or more aryl or heteroaryl groups may also be linked by a non-aromatic unit, for example by a carbon, nitrogen or oxygen atom. For example, in the context of the present invention, also systems such as fluorene, 9,9' -spirobifluorene, 9,9-diarylfluorene, triarylamines, diaryl ethers, stilbenes, etc. should be considered as aromatic ring systems, and also systems in which two or more aryl groups are connected by, for example, short alkyl groups. Preferably, the aromatic ring system is selected from fluorene, 9,9' -spirobifluorene, 9,9-diarylamine or a group in which two or more aryl and/or heteroaryl groups are connected to each other by single bonds.

In the context of the present invention, may contain 1 to 20 carbon atoms and wherein individual hydrogen atoms or CH ₂ An aliphatic hydrocarbon radical or alkyl radical or alkenyl or alkynyl radical which is also substituted by the abovementioned radicals is preferably understood as meaning a methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, 2-methylbutyl, n-pentyl, sec-pentyl, neopentyl, cyclopentyl, n-hexyl, neohexyl, cyclohexyl, n-heptyl, cycloheptyl, n-octyl, cyclooctyl, 2-ethylhexyl, trifluoromethyl, pentafluoroethyl, 2,2,2-trifluoroethyl, vinyl, propenyl, butenyl, pentenyl, cyclopentenyl, hexenyl, cyclohexenyl, heptenyl, cycloheptenyl, octenyl, cyclooctenyl, ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl or octynyl radical. Alkoxy radicals having from 1 to 40 carbon atoms are preferably understood as meaning methoxy, trifluoromethoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy, n-pentoxy, sec-pentoxy, 2-methylbutoxy, n-hexoxy, cyclohexoxy, n-heptoxy, cycloheptoxy, n-octoxy, cyclooctoxy, 2-ethylhexoxy, pentafluoroethoxy and 2,2,2-trifluoroethoxy. Thioalkyl having 1 to 40 carbon atoms is understood as meaning in particular methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio, tert-butylthio, n-pentylthio, sec-pentylthio, n-hexylthio, cyclohexylthio, n-heptylthio, cycloheptylthio, n-octylthio, cyclooctylthio, 2-ethylhexylthio, trifluoromethylthio, pentafluoroethylthio, 2,2,2-trifluoroethylthio, vinylthio, propenylthio, butenylthio, pentenylthio, cyclopentenylthio, hexenylthio, cyclohexenylthio, heptenylthio, cycloheptenylthio, octenylthio, cyclooctenylthio, ethynylthio, propynylthio, butynylthio, pentynylthio, hexynylthio, heptynylthio or octynylthio. In general, alkyl, alkoxy orThe thioalkyl groups may be straight-chain, branched or cyclic, in which one or more non-adjacent CH' s ₂ The groups may be replaced by the above groups; furthermore, one or more hydrogen atoms may also be replaced by D, F, cl, br, I, CN or NO ₂ Instead, it can preferably be replaced by F, cl or CN, preferably also by F or CN, particularly preferably by CN.

Aromatic or heteroaromatic ring systems which have from 5 to 60 or from 5 to 40 aromatic ring atoms and can in each case also be substituted by the abovementioned radicals and can be attached to the aromatic or heteroaromatic system via any desired position are to be understood as meaning in particular radicals which originate from: benzene, naphthalene, anthracene, benzanthracene, phenanthrene, pyrene, chicory, perylene, fluoranthene, tetracene, pentacene, benzopyrene, biphenyl, dibenzylidene, terphenyl, bistriphenylidene, fluorene, spirobifluorene, dihydrophenanthrene, dihydropyrene, tetrahydropyrene, cis-or trans-indenofluorene, cis-or trans-indenocarbazole, cis-or trans-indolocarbazole, triindene, isotridecyl, spirotriindene, spiroisotridecyl, furan, benzofuran, isobenzofuran, dibenzofuran, thiophene, benzothiophene, isobenzothiophene, dibenzothiophene, pyrrole, indole, isoindole, carbazole, pyridine, quinoline, isoquinoline, acridine, phenanthridine, benzo-5,6-quinoline, benzo-6,7-quinoline, benzo-7,8-quinoline, phenothiazine, thiophene

Oxazines, pyrazoles, indazoles, imidazoles, benzimidazoles, naphthoimidazoles, phenanthroimidazoles, pyridoimidazoles, pyrazinoimidazoles, quinoxalimidazoles, benzoxazoles,

Azole, benzo

Azoles, naphtho

Azoles, anthracenes

Azole, phenanthro

Oxazole, iso

Oxazole, 1,2-thiazole, 1,3-thiazole, benzothiazole, pyridazine, hexaazaterphenyl, benzopyridazine, pyrimidine, benzopyrimidine, quinoxaline, 1,5-diaza anthracene, 2,7-diaza pyrene, 2,3-diaza pyrene, 1,6-diaza pyrene, 1,8-diaza pyrene, 4,5-diaza pyrene, 4,5,9,10-tetraazaperylene, pyrazine, phenazine, thiophene

Oxazines, phenothiazines, fluorarenes, naphthyridines, azacarbazoles, benzocarbazoles, phenanthrolines, 1,2,3-triazole, 1,2,4-triazole, benzotriazole, 1,2,3-

Oxadiazole 1,2,4-

Oxadiazole 1,2,5-

Oxadiazole 1,3,4-

Oxadiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,2,5-thiadiazole, 1,3,4-thiadiazole, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, tetrazole, 1,2,4,5-tetrazine, 1,2,3,4-tetrazine, 1,2,3,5-tetrazine, purine, pteridine, indolizine and benzothiadiazole, or groups derived from combinations of these systems.

In the context of the present specification, the wording that two or more groups may together form a ring should be understood to mean in particular that the two groups are linked to each other by a chemical bond formally eliminating two hydrogen atoms. This is illustrated by the following scheme:

however, in addition, the above wording is also understood to mean that if one of the two groups is hydrogen, the second group is bonded to the position to which the hydrogen atom is originally bonded, thereby forming a ring. This will be illustrated by the following scheme:

in a preferred arrangement, the compounds of the present invention may comprise structures of formulae (IIa) to (IIk); more preferably, the compounds of the invention may be selected from compounds of formulae (IIa) to (IIk):

wherein W ¹ 、W ² 、Y ¹ 、Y ² 、Z ¹ 、Z ² 、X ¹ 、X ² And X ³ Having the definitions given above, in particular for formula (I), and the other symbols and indices are as follows:

x is identical or different on each occurrence and X is N, CR, or if p is 1, X is C, preferably X is CR or C, provided that no more than two X groups in a ring are N;

Y ³ in each case the same or differentAnd is O, S, N (Ar'), N (R), C = O, C (R) ₂ 、Si(R) ₂ 、C＝NR、C＝NAr'、C＝C(R) ₂ B (Ar') or B (R), preferably C (R) ₂ O, S or N (Ar');

p is 0 or 1.

In another preferred embodiment, it is possible that the compounds of the invention comprise structures of formulae (IIIa) to (IIIk), wherein the compounds of the invention may more preferably be selected from compounds of formulae (IIIa) to (IIIk),

wherein the symbol Y ¹ 、Y ² 、Z ¹ 、Z ² 、X ¹ 、X ² And X ³ Having the definitions given above, in particular for formula (I), the symbol X, Y ³ And the subscript p has the definitions given above, especially for formulae (IIa) to (IIk).

It may be preferred that in formulae (I), (IIa) to (IIk) and/or (IIIa) to (IIIk) not more than four, preferably not more than two X, X ¹ 、X ² And X ³ The group is N; more preferably, if X and X ³ The groups form a ring system by bonding, all X, X ¹ 、X ² And X ³ The radicals are all CR and CR ^a 、CR ^b 、CR ^c Or C.

In another preferred embodiment, it may be the case that the compounds of the present invention comprise structures of formulae (IV-1) to (IV-20), wherein the compounds of the present invention may be more preferably selected from compounds of formulae (IV-1) to (IV-20),

wherein the symbol Y ¹ 、Y ² 、Z ¹ 、Z ² 、R、R ^a 、R ^b And R ^c Having the definitions given above, especially for formula (I), the symbol Y ³ Having the definitions given above, in particular for formulae (IIa) to (IIk), subscript l is 0, 1,2,3,4 or 5, preferably 0, 1 or 2, subscript m is 0, 1,2,3 or 4, preferably 0, 1 or 2, subscript n is 0, 1,2 or 3, preferably 0, 1 or 2, subscript j is 0, 1 or 2, preferably 0 or 1, subscript k is 0 or 1.

Preference is given here to structures/compounds of the formulae (IV-1) to (IV-10), particular preference to structures of the formulae (IV-1) to (IV-9).

In the structures/compounds of the formulae (IV-1) to (IV-20), the sum of the indices j, l, m and n is preferably not more than 8, particularly preferably not more than 6, very particularly preferably not more than 4.

Furthermore, in preferred embodiments of the formulae (I), (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20) and/or in particular those formulae which are set forth below, it is possible: z is a linear or branched member ¹ And Z ² At least one, preferably two, of the radicals being N, Y ¹ And Y ² At least one, preferably two, of the radicals is B (Ar), B (R), P (= O) Ar, P (= O) R, al (Ar), al (R), ga (Ar), ga (R), C = O, S = O or SO ₂ Preferably, C = O, B (Ar), B (R), P (= O) Ar, P (= O) R, C = O, S = O or SO ₂ More preferably, C =O, B (R) or B (Ar). Wherein Z ¹ And Z ² At least one of the radicals is N, and at least one, preferably two, Y ¹ 、Y ² The groups are B (Ar), B (R), P (= O) Ar, P (= O) R, al (Ar), al (R), ga (Ar), ga (R), C = O, S = O or SO ₂ Can advantageously be used as a luminaire.

Furthermore, in the preferred embodiments of the formulae (I), (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20) and/or in particular those illustrated below, it is possible that: z ¹ And Z ² At least one, preferably two, of the radicals are N and Y ¹ And Y ² At least one, preferably two, of the groups is N (Ar), N (R), P (Ar), P (R), O, S or Se, preferably N (Ar), N (R), O or S, more preferably N (Ar).

Wherein Z ¹ And Z ² At least one, preferably two, of the radicals are N and Y ¹ 、Y ² Embodiments in which at least one, preferably two, of the groups are N (Ar), N (R), P (Ar), P (R), O, S, or Se, may be particularly advantageously used as hole conductor materials.

In a further configuration, in the formulae (I), (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20) and/or in particular in the preferred embodiments of these formulae set forth below, it is possible that: z ¹ And Z ² At least one, preferably two, of the radicals is B and Y ¹ 、Y ² At least one, preferably two, of the groups is N (Ar), N (R), P (Ar), P (R), O, S or Se, preferably N (Ar), N (R), O or S, more preferably N (Ar). Z ¹ And Z ² At least one of the radicals is B and at least one, preferably two, Y ¹ 、Y ² Configurations in which the radicals are N (Ar), N (R), P (Ar), P (R), O, S or Se can be advantageously used as luminophores.

In a further configuration, in the formulae (I), (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20) and/or in particular in the preferred embodiments of these formulae set forth below, it is possible that: z ¹ And Z ² At least one, preferably two, of the radicals are B, and Y ¹ 、Y ² At least one of the radicalsPreferably, two are B (Ar), B (R), P (= O) Ar, P (= O) R, al (Ar), al (R), ga (Ar), ga (R), C = O, S = O or SO ₂ Preferably, C = O, B (Ar), B (R), P (= O) Ar, P (= O) R, C = O, S = O or SO ₂ More preferably C = O, B (R) or B (Ar).

Wherein Z ¹ And Z ² At least one, preferably two, of the radicals is B and Y ¹ 、Y ² At least one, preferably two, of the radicals is B (Ar), B (R), P (= O) Ar, P (= O) R, al (Ar), al (R), ga (Ar), ga (R), C = O, S = O or SO ₂ Embodiments of (a) can be used particularly advantageously as an electron transport material.

Furthermore, in preferred embodiments of the formulae (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20) and/or in particular of the formulae detailed below, it is possible for two Y's to be present ³ The groups are the same.

Furthermore, in preferred embodiments of the formulae (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20) and/or in particular of these formulae detailed below, it is possible for two Y's to be present ³ The groups are different.

More preferably, the compound comprises at least one structure of formulae (V-1) to (V-40); more preferably, the compound is selected from compounds of formulae (V-1) to (V-40):

wherein the symbol Z ¹ 、Z ² 、X、X ¹ And X ² Having the definitions given above, especially for formula (I), the symbol Y ³ Having the definitions given above, especially for the formulae (IIa) to (IIk), Z ³ 、Z ⁴ Identical or different in each case and is N, B, P (= O) or Si (R), preferably N, B or P (= O), more preferably N or B.

Preference is given here to structures/compounds of the formulae (V-1) to (V-30), particular preference to structures of the formulae (V-2), (V-5) to (V-9), (V-12), (V-15) to (V-19), (V-22), (V-25) to (V-29).

It may also be the case that, in the formulae (V-1) to (V-40), not more than four, preferably not more than two, X, X ¹ And X ² The group is N; more preferably, all X, X ¹ And X ² The radicals are all CR, CR ^a 、CR ^b All X, X if they form a closed ring with the X group by a bond ¹ And X ² The radical is C.

More preferably, the compound comprises at least one structure of formulae (VI-1) to (VI-40); more preferably, the compound is selected from compounds of formulae (VI-1) to (VI-40):

wherein the symbol Z ¹ 、Z ² 、R、R ^a And R ^b Having the definitions given above, especially for formula (I), the symbol Y ³ Having the definitions given above, especially for the formulae (IIa) to (IIk), Z ³ 、Z ⁴ Identical or different in each case and is N, B, P (= O) or Si (R), preferably N, B or P (= O), more preferably N or B, subscript l is 0, 1,2,3,4 or 5, preferably 0, 1 or 2, subscript m is 0, 1,2,3 or 4, preferably 0, 1 or 2, subscript j is 0, 1 or 2, preferably 0 or 1.

Preference is given here to structures/compounds of the formulae (VI-1) to (VI-30), particular preference to structures/compounds of the formulae (VI-2), (VI-5) to (VI-9), (VI-12), (VI-15) to (VI-19), (VI-22), (VI-25) to (VI-29).

Furthermore, in preferred embodiments of the formulae (V-1) to (V-20), (VI-1) to (VI-20) and/or in particular of these formulae detailed below, it is possible: z ¹ And Z ² At least one, preferably two of the radicals are N, and Z ³ And Z ⁴ At least one, preferably two of the radicals are B. Wherein Z ¹ And Z ² At least one, preferably two, of the radicals are N, and Z ³ And Z ⁴ An arrangement in which at least one, preferably both, of the radicals is B can advantageously be used as luminophore.

Furthermore, in preferred embodiments of the formulae (V-1) to (V-20), (VI-1) to (VI-20) and/or in particular of these formulae detailed below, it is possible that: z ¹ And Z ² At least one, preferably two, of the radicalsIs N, and Z ³ And Z ⁴ At least one, preferably two of the radicals are N.

Wherein Z ¹ 、Z ² 、Z ³ 、Z ⁴ Embodiments in which many, preferably all, of the groups are N can be used particularly advantageously as hole conductor materials.

In another configuration, in preferred embodiments of formulae (V-1) to (V-20), (VI-1) to (VI-20) and/or in particular of these formulae detailed below, it is possible that: z ¹ And Z ² At least one, preferably two, of the radicals are B, and Z ³ And Z ⁴ At least one, preferably two, of the radicals are N. Wherein Z ¹ And Z ² At least one, preferably two of the radicals are B, and Z ³ And Z ⁴ An arrangement in which at least one, preferably both, of the radicals is N can advantageously be used as luminophore.

In another configuration, in preferred embodiments of formulae (V-1) to (V-20), (VI-1) to (VI-20) and/or in particular of these formulae detailed below, it is possible that: z is a linear or branched member ¹ And Z ² At least one, preferably two, of the radicals are B, and Z ³ And Z ⁴ At least one, preferably two of the radicals are B.

Wherein Z ¹ 、Z ² 、Z ³ 、Z ⁴ Embodiments in which many, preferably all, of the groups are B may be particularly advantageously used as electron transport materials.

In another configuration, in preferred embodiments of formulae (V-1) to (V-20), (VI-1) to (VI-20) and/or in particular of those formulae detailed below, it is possible that: z is a linear or branched member ² 、Z ³ At least one, preferably two of the radicals are N, and Z ⁴ 、Z ⁵ At least one, preferably two of the radicals are B.

In the structures of formulae (VI-1) to (VI-40), it is possible that: the sum of the indices j, l and m is preferably not more than 8, particularly preferably not more than 6, very particularly preferably not more than 4.

In a preferred development of the invention, it is possible that: at least two R, R ^a 、R ^b 、R ^c The sum of radicals and the two R, R ^a 、R ^b 、R ^c The additional groups to which the groups are attached together form a fused ring, wherein the two R, R ^a 、R ^b 、R ^c The groups form at least one structure of formulae (RA-1) to (RA-12):

wherein R is ¹ Having the above definition, the dashed bonds represent the two R, R ^a 、R ^b 、R ^c The attachment site to which the group binds, and other symbols are defined as follows:

Y ⁴ in each case identical or different, and is C (R) ¹ ) ₂ 、(R ¹ ) ₂ C-C(R ¹ ) ₂ 、(R ¹ )C＝C(R ¹ )、NR ¹ NAr', O or S, preferably C (R) ¹ ) ₂ 、(R ¹ ) ₂ C-C(R ¹ ) ₂ 、(R ¹ )C＝C(R ¹ ) O or S;

R ^d identical or different on each occurrence and is F, a straight-chain alkyl, alkoxy or thioalkoxy group having from 1 to 40 carbon atoms or an alkenyl or alkynyl group having from 2 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having from 3 to 20 carbon atoms, where the alkyl, alkoxy, thioalkoxy, alkenyl or alkynyl group can in each case be substituted by one or more R ² Radical substitution of one or more non-adjacent CH ₂ The group can be represented by R ² C＝CR ² 、C≡C、Si(R ² ) ₂ 、C＝O、C＝S、C＝Se、C＝NR ² 、-C(＝O)O-、-C(＝O)NR ² -、NR ² 、P(＝O)(R ¹ ) -O-, -S-, SO or SO ₂ Instead of, or with 5 to 60 aromatic ring atoms andand may in each case be substituted by one or more R ² Aromatic or heteroaromatic ring systems substituted by radicals, or having 5 to 60 aromatic ring atoms and which may be substituted by one or more R ² A group-substituted aryloxy or heteroaryloxy group; at the same time, two R ^d The radicals together or one R ^d Group and R ¹ The radicals together or with further radicals may also form a ring system;

s is 0, 1,2,3,4, 5 or 6, preferably 0, 1,2,3 or 4, more preferably 0, 1 or 2;

t is 0, 1,2,3,4, 5,6, 7 or 8, preferably 0, 1,2,3 or 4, more preferably 0, 1 or 2;

v is 0, 1,2,3,4, 5,6, 7,8 or 9, preferably 0, 1,2,3 or 4, more preferably 0, 1 or 2.

In a preferred embodiment of the invention, at least two R, R ^a 、R ^b 、R ^c The sum of radicals and the two R, R ^a 、R ^b 、R ^c The additional groups to which the groups are attached together form a fused ring, wherein the two R, R ^a 、R ^b 、R ^c The radicals preferably form at least one structure of the formulae (RA-1 a) to (RA-4 f):

wherein the dashed bonds represent the two R, R ^a 、R ^b 、R ^c The subscript m is 0, 1,2,3 or 4, preferably 0, 1 or 2, and the symbol R is ¹ 、R ² 、R ^d And the subscripts s and t have the definitions given above especially for formula (I) and/or formulae (RA-1) to (RA-12).

It may also be the case that at least two R, R which form structures of formulae (RA-1) to (RA-12) and/or (RA-1 a) to (RA-4 f) and form fused rings ^a 、R ^b 、R ^c The radicals are derived from the adjacent X, X ¹ 、X ² 、X ³ Radical R, R ^a 、R ^b 、R ^c Or represents R groups each bound to an adjacent carbon atom, wherein these carbon atoms are preferably linked by a bond.

In a more preferred configuration, at least two R, R ^a 、R ^b 、R ^c The sum of radicals and the two R, R ^a 、R ^b 、R ^c The additional groups to which the groups are attached together form a fused ring, wherein the two R, R ^a 、R ^b 、R ^c The group forms a structure of formula (RB):

wherein R is ¹ Having the definitions given above, in particular for formula (I), the dashed bonds represent the two R, R ^a 、R ^b 、R ^c The subscript m is 0, 1,2,3, or 4, preferably 0, 1, or 2,Y, the attachment site to which the group is attached ⁵ Is C (R) ¹ ) ₂ 、NR ¹ 、NAr'、BR ¹ BAr', O or S, preferably C (R) ¹ ) ₂ NAr' or O.

It is possible that at least two R, R form structures of formula (RB) and form fused rings ^a 、R ^b 、R ^c The radicals are derived from the adjacent X, X ¹ 、X ² 、X ³ Group R, R ^a 、R ^b 、R ^c Or represent R groups each bound to an adjacent carbon atom, wherein these carbon atoms are preferably linked to each other by a bond.

More preferably, the compound comprises at least one structure of formulae (VII-1) to (VII-50); more preferably, the compound is selected from compounds of formulae (VII-1) to (VII-50), wherein the compounds have at least one fused ring:

wherein the symbol Y ¹ 、Y ² 、Z ¹ 、Z ² 、R、R ^a 、R ^b And R ^c Having the definitions given above, especially for formula (I), the symbol Y ³ Having the definitions given above, in particular for formulae (IIa) to (IIk), the symbol o denotes a fused ring attachment site and the other symbols are defined as follows:

l is 0, 1,2,3,4 or 5, preferably 0, 1 or 2;

m is 0, 1,2,3 or 4, preferably 0, 1 or 2;

n is 0, 1,2 or 3, preferably 0, 1 or 2;

j is 0, 1 or 2, preferably 0 or 1;

k is 0 or 1.

Preferably, the fused rings, especially in formulae (VII-1) to (VII-50), are fused via at least two R, R ^a 、R ^b 、R ^c Group and the compoundsTwo R, R ^a 、R ^b 、R ^c Additional groups of groups bound, at least two of which are R, R ^a 、R ^b 、R ^c The radicals form structures of the formulae (RA-1) to (RA-12), (RA-1 a) to (RA-4 f) and/or (RB), preferably of the formulae (RA-1) to (RA-12) and/or (RA-1 a) to (RA-4 f).

Possible preferences are that the compounds have at least two fused rings, wherein at least one fused ring is formed by a structure of formulae (RA-1) to (RA-12) and/or (RA-1 a) to (RA-4 f) and another ring is formed by a structure of formulae (RA-1) to (RA-12), (RA-1 a) to (RA-4 f) or (RB), wherein the compounds comprise at least one structure of formulae (VIII-1) to (VIII-50), preferably wherein the compounds are selected from compounds of formulae (VIII-1) to (VIII-50):

wherein the symbol Y ¹ 、Y ² 、Z ¹ 、Z ² 、R、R ^a 、R ^b And R ^c Having the definitions given above, especially for formula (I), the symbol Y ³ Having the definitions given above, in particular for formulae (IIa) to (IIk), the symbol o denotes the attachment site, and the other symbols have the following definitions:

l is 0, 1,2,3,4 or 5, preferably 0, 1 or 2;

m is 0, 1,2,3 or 4, preferably 0, 1 or 2;

n is 0, 1,2 or 3, preferably 0, 1 or 2;

j is 0, 1 or 2, preferably 0 or 1; and

k is 0 or 1.

In particular in formulae (VII-1) to (VII-50) and/or (VIII-1) to (VIII-50), the sum of the indices k, j, l, m and n is preferably 0, 1,2 or 3, more preferably 1 or 2.

The possible scenarios here are: the formulae (VIII-1) to (VIII-50) have at least two fused rings, wherein the fused rings are identical and consist of two R, R ^a 、R ^b 、R ^c The moiety formed by the group may be represented by at least one of the structures of formulae (RA-1) to (RA-12) and/or (RA-1 a) to (RA-4 f).

It is also possible that: the formulae (VIII-1) to (VIII-50) have at least two fused rings, wherein the fused rings are different and consist of two R, R ^a 、R ^b 、R ^c The moiety formed by the group can be represented in each case by at least one structure of the formulae (RA-1) to (RA-12) and/or (RA-1 a) to (RA-4 f).

Further possible situations are: the formulas (VIII-1) to (VIII-50) have at least two fused rings, wherein the fused rings are different and one of the two fused rings has a fused ring structure consisting of two R, R ^a 、R ^b 、R ^c A moiety formed by a group, which moiety can be represented by at least one of the structures of formulae (RA-1) to (RA-12) and/or (RA-1 a) to (RA-4 f), and one of the two fused rings has two R, R ^a 、R ^b 、R ^c A moiety formed by a group, which moiety may be of the structure of formula (RB)One is shown.

Further possible situations are: substituent R, R according to the above formula ^a 、R ^b 、R ^c And R ^d 、R ¹ And R ² Not substituted R, R ^a 、R ^b 、R ^c And R ^d 、R ¹ And R ² The ring atoms of the ring system to which they are attached form a fused aromatic or heteroaromatic ring system. This includes bonding to R, R ^a 、R ^b 、R ^c 、R ^d And R ¹ Possible substituents R of the radicals ¹ And R ² Forming a fused aromatic or heteroaromatic ring system.

But may be selected from R, R ^a 、R ^b 、R ^c 、R ^d 、R ¹ And/or R ² When two radicals form a ring system with one another, the ring system may be monocyclic or polycyclic, aliphatic, heteroaliphatic, aromatic or heteroaromatic. In this case, the groups which together form a ring system may be adjacent, which means that these groups are bonded to the same carbon atom or to carbon atoms which are directly bonded to one another, or they may also be removed from one another. Further, has a substituent R, R ^a 、R ^b 、R ^c 、R ^d 、R ¹ And/or R ² The ring systems of (a) may also be linked to each other by a bond, which may thus result in ring closure. In this case, each of the respective attachment sites preferably has a substituent R, R ^a 、R ^b 、R ^c 、R ^d 、R ¹ And/or R ² 。

In a preferred configuration, the compounds of the present invention can be represented by at least one of the structures of formulae (I), (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20), (V-1) to (V-40), (VI-1) to (VI-40), (VII-1) to (VII-50) and/or (VIII-1) to (VIII-50). Preferably, the compounds of the invention, preferably comprising structures of the formulae (I), (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20), (V-1) to (V-40), (VI-1) to (VI-40), (VII-1) to (VII-50) and/or (VIII-1) to (VIII-50), have a molecular weight of not more than 5000g/mol, preferably not more than 4000g/mol, particularly preferably not more than 3000g/mol, particularly preferably not more than 2000g/mol, most preferably not more than 1200 g/mol.

Furthermore, a feature of preferred compounds of the invention is that they are sublimable. These compounds generally have a molar mass of less than about 1200 g/mol.

Preferred aromatic or heteroaromatic ring systems R, R ^a 、R ^b 、R ^c 、R ^d Ar' and/or Ar are selected from phenyl, biphenyl, in particular ortho-, meta-or para-biphenyl, terphenyl, in particular ortho-, meta-or para-terphenyl or branched terphenyl, quaterphenyl, in particular ortho-, meta-or para-quaterphenyl or branched quaterphenyl, fluorenyl which can be connected via the 1-, 2-, 3-or 4-position, spirobifluorene which can be connected via the 1-, 2-, 3-or 4-position, naphthalene, in particular 1-or 2-bonded naphthalene, indole, benzofuran, benzothiophene, carbazole which can be connected via the 1-, 2-, 3-, 4-or 9-position, dibenzofuran which can be connected via the 1-, 2-, 3-or 4-position, dibenzothiophene which can be connected via the 1-, 2-, 3-or 4-position, indolocarbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinoline, isoquinoline, quinazoline, quinoline, quinazoline

Phenanthrene or triphenylene, each of which may be substituted by one or more R ¹ Or R groups.

The preferred cases that are possible are: at least one substituent R, R ^a 、R ^b 、R ^c In each case identical or different and selected from H, D, branched or cyclic alkyl, alkoxy or thioalkoxy groups having from 3 to 20 carbon atoms, or from aromatic or heteroaromatic ring systems of the formula Ar-1 to Ar-75, where the substituents R, R ^a 、R ^b 、R ^c Preferably a ring forming a structure according to formulae (RA-1) to (RA-12), (RA-1 a) to (RA-4 f) or (RB), or a substituent R, R ^a 、R ^b 、R ^c Identical or different on each occurrence and selected from H, D or an aromatic or heteroaromatic ring system selected from the group of the formulae Ar-1 to Ar-75 below, and/or the Ar' group is inIn each case identical or different and selected from the group of formulae Ar-1 to Ar-75:

wherein R is ¹ As defined above, the dashed bonds represent attachment sites, and further:

Ar ¹ are identical or different on each occurrence and are each having from 6 to 18 aromatic ring atoms and may be substituted in each case by one or more R ¹ A divalent aromatic or heteroaromatic ring system substituted with a group;

a is identical or different on each occurrence and is C (R) ¹ ) ₂ 、NR ¹ O or S;

p is 0 or 1, wherein p =0 represents Ar ¹ The radicals being absent, the corresponding aromatic or heteroaromatic radicals being bonded directly to the corresponding radicals;

q is 0 or 1, wherein q =0 indicates that no A group is bonded at this position, but R ¹ The groups are bonded to the corresponding carbon atoms.

When the above groups of Ar have two or more a groups, possible choices of these groups include all combinations of the definitions of a. In this case, a preferred embodiment is one in which one A group is NR ¹ The other A group is C (R) ¹ ) ₂ Or wherein both A groups are NR ¹ Or those in which both A groups are O.

When A is NR ¹ When bonded to a nitrogen atom ¹ Preferably having 5 to 24 aromatic ring atoms and which may also be interrupted by one or more R ² A group-substituted aromatic or heteroaromatic ring system. In a particularly preferred embodiment, the R is ¹ The substituents are identical or different on each occurrence and are aromatic or heteroaromatic ring systems having from 6 to 24 aromatic ring atoms, in particular from 6 to 18 aromatic ring atoms, which do not have any fused aryl groups and which do not have any fused heteroaryl groups in which two or more aromatic or heteroaromatic 6-membered ring groups are fused directly to one another and which may also be substituted by one or more R in each case ² And (4) substituting the group. Phenyl, biphenyl, terphenyl, and quaterphenyl groups having the bonding patterns as set forth above for Ar-1 to Ar-11 are preferred, wherein these structures are not substituted with R ¹ Substituted but can be substituted by one or more R ² Substituted, but preferably unsubstituted. Also preferred are triazines, pyrimidines and quinazolines as set forth above for Ar-47 through Ar-50, ar-57 and Ar-58, wherein these structures are not substituted with R ¹ Instead, it may be substituted by one or more R ² And (4) substituting the group.

Preferred substituents R, R are described below ^a 、R ^b 、R ^c And R ^d 。

In a preferred embodiment of the invention, R, R ^a 、R ^b 、R ^c In each case identical or different and selected from H, D, F, CN, NO ₂ ，Si(R ¹ ) ₃ ，B(OR ¹ ) ₂ Straight-chain alkyl groups having 1 to 20 carbon atoms or branched or cyclic alkanes having 3 to 20 carbon atomsRadical, where the alkyl radical may in each case be substituted by one or more R ¹ Substituted by radicals or having 5 to 60 aromatic ring atoms, preferably 5 to 40 aromatic ring atoms and can in each case be substituted by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system.

In another preferred embodiment of the present invention, the substituent R, R ^a 、R ^b 、R ^c Are identical or different on each occurrence and are selected from H, D, F, linear alkyl radicals having from 1 to 20 carbon atoms or branched or cyclic alkyl radicals having from 3 to 20 carbon atoms, where the alkyl radicals may in each case be substituted by one or more R ¹ Substituted by radicals, or having 5 to 60 aromatic ring atoms, preferably 5 to 40 aromatic ring atoms and may in each case be substituted by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system.

It is also possible that: at least one substituent R, R ^a 、R ^b 、R ^c In each case identical or different and selected from H, D, having from 6 to 30 aromatic ring atoms and which may be substituted by one or more R ¹ Radical-substituted aromatic or heteroaromatic ring systems or N (Ar') ₂ A group. In another preferred embodiment of the invention, substituent R, R ^a 、R ^b 、R ^c A ring forming a structure according to formulae (RA-1) to (RA-12), (RA-1 a) to (RA-4 f), or (RB), or R, R ^a 、R ^b 、R ^c Identical or different in each case and selected from H, D, having 6 to 30 aromatic ring atoms and which may be substituted by one or more R ¹ Radical-substituted aromatic or heteroaromatic ring systems or N (Ar') ₂ A group. More preferably, substituent R, R ^a 、R ^b 、R ^c Identical or different on each occurrence and selected from H or an aromatic or heteroaromatic ring system having from 6 to 24 aromatic ring atoms, preferably from 6 to 18 aromatic ring atoms, more preferably from 6 to 13 aromatic ring atoms, each of which may be interrupted by one or more R ¹ And (4) substituting the group.

In a preferred embodiment of the invention, R ^d At each kindAre identical or different and are selected from linear alkyl groups having from 1 to 20 carbon atoms or branched or cyclic alkyl groups having from 3 to 20 carbon atoms, where the alkyl groups can in each case be substituted by one or more R ¹ Substituted by groups; or having from 5 to 60 aromatic ring atoms, preferably from 5 to 40 aromatic ring atoms, and may in each case be substituted by one or more R ¹ Substituted aromatic or heteroaromatic ring systems.

In another preferred embodiment of the present invention, R ^d Are identical or different on each occurrence and are selected from linear alkyl radicals having from 1 to 10 carbon atoms or branched or cyclic alkyl radicals having from 3 to 10 carbon atoms, where the alkyl radicals may in each case be substituted by one or more R ¹ Substituted by radicals having 6 to 30 aromatic ring atoms and which may be substituted by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system. More preferably, R ^a Are identical or different on each occurrence and are selected from linear alkyl radicals having from 1 to 5 carbon atoms or branched or cyclic alkyl radicals having from 3 to 5 carbon atoms, where the alkyl radicals may in each case be substituted by one or more R ¹ Substituted by radicals, or having 6 to 24 aromatic ring atoms, preferably 6 to 18 aromatic ring atoms, more preferably 6 to 13 aromatic ring atoms, and may in each case be substituted by one or more R ¹ A substituted aromatic or heteroaromatic ring system.

In a preferred embodiment of the invention, R ^d Are identical or different on each occurrence and are selected from linear alkyl radicals having from 1 to 6 carbon atoms or cyclic alkyl radicals having from 3 to 6 carbon atoms, where the alkyl radicals may in each case be substituted by one or more R ¹ Substituted by radicals, or having 6 to 24 aromatic ring atoms and may in each case be substituted by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system; at the same time, two R ^d The radicals may also together form a ring system. More preferably, R ^d In each case identical or different and are selected from linear alkyl radicals having 1,2,3 or 4 carbon atoms or branched chains having 3 to 6 carbon atomsOr cyclic alkyl groups, wherein the alkyl group may in each case be interrupted by one or more R ¹ A group, but preferably unsubstituted, or have 6 to 12 aromatic ring atoms, especially 6 aromatic ring atoms, and may in each case be substituted by one or more, more preferably non-aromatic R ¹ A substituted, but preferably unsubstituted, aromatic ring system; at the same time, two R ^d The groups may together form a ring system. Most preferably, R ^d In each case identical or different and are selected from straight-chain alkyl radicals having 1,2,3 or 4 carbon atoms or branched alkyl radicals having 3 to 6 carbon atoms. Most preferably, R ^d Is a methyl group or a phenyl group, wherein two phenyl groups may together form a ring system, preferably a methyl group as compared to a phenyl group.

Preferred aromatic or heteroaromatic ring system substituent R, R ^a 、R ^b 、R ^c 、R ^d Or Ar' is selected from phenyl, biphenyl, especially ortho-, meta-or para-biphenyl, terphenyl, especially ortho-, meta-or para-terphenyl or branched terphenyl, quaterphenyl, especially ortho-, meta-or para-quaterphenyl or branched quaterphenyl, fluorene which may be linked through the 1-, 2-, 3-or 4-position, spirobifluorene which may be linked through the 1-, 2-, 3-or 4-position, naphthalene, especially 1-or 2-bonded naphthalene, indole, benzofuran, benzothiophene, carbazolyl which may be linked through the 1-, 2-, 3-or 4-position, dibenzofuran which may be linked through the 1-, 2-, 3-or 4-position, dibenzothiophene which may be linked through the 1-, 2-, 3-or 4-position, indenocarbazole, indolocarbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinoline, isoquinoline, quinazoline, indolocarbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, quinoline, isoquinoline, quinazoline, terphenyl, or branched terphenyl

Phenanthryl or triphenylidene, each of which may be substituted by one or more R, R ¹ Or R ² And (4) substituting the group. The structures Ar-1 to Ar-75 listed above are particularly preferred, with preference given to compounds of the formulae (Ar-1), (Ar-2), (Ar-3), (Ar-12), (Ar-13), (Ar-14), (Ar-15), (Ar-16), (Ar-69), (Ar-7)0) (Ar-75), particularly preferably represented by the formulae (Ar-1), (Ar-2), (Ar-3), (Ar-12), (Ar-13), (Ar-14), (Ar-15) and (Ar-16). With respect to structures Ar-1 to Ar-75, it should be noted that they are shown as having substituent R ¹ . In the case of ring systems Ar, these substituents R ¹ Should be replaced by R, at R ^d In the case of (A), these substituents R ¹ Should be substituted by R ² Instead.

Another suitable R, R ^a 、R ^b 、R ^c The radical being of the formula-Ar ⁴ -N(Ar ² )(Ar ³ ) Group of (1), wherein Ar ² 、Ar ³ And Ar ⁴ Are identical or different on each occurrence and are of 5 to 24 aromatic ring atoms and may be substituted in each case by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system. Ar here ² 、Ar ³ And Ar ⁴ The total number of aromatic ring atoms in the ring does not exceed 60, preferably 40.

In this case, by selecting from C (R) ¹ ) ₂ 、NR ¹ Radicals of O and S, ar ⁴ And Ar ² May also be bonded to each other and/or Ar ² And Ar ³ And may be bonded to each other. Preferably, ar is in the corresponding ortho position bonded to the nitrogen atom ⁴ And Ar ² Are connected to each other and Ar ² And Ar ³ Are connected to each other. In another embodiment of the present invention, ar ² 、Ar ³ And Ar ⁴ None of the groups are bonded to each other.

Preferably, ar ⁴ Are of 6 to 24 aromatic ring atoms, preferably of 6 to 12 aromatic ring atoms, and may in each case be substituted by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system. More preferably, ar ⁴ Selected from ortho-, meta-or para-phenylene or ortho-, meta-or para-biphenyl, each of which may be substituted with one or more R ¹ The radicals are substituted, but preferably unsubstituted. Most preferably, ar ⁴ Is an unsubstituted phenylene radical.

Preferably, ar ² And Ar ³ In each case the same or different, andare of 6 to 24 aromatic ring atoms and may be substituted in each case by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system. Particularly preferred Ar ² And Ar ³ The radicals are identical or different on each occurrence and are selected from the group consisting of benzene, o-biphenyl, m-biphenyl or p-biphenylyl, o-terphenyl, m-terphenyl or p-terphenyl or branched terphenyl, o-quaterphenyl, m-or p-quaterphenyl or branched quaterphenyl, 1-fluorenyl, 2-fluorenyl, 3-fluorenyl or 4-fluorenyl, 1-spirobifluorenyl, 2-spirobifluorenyl, 3-spirobifluorenyl or 4-spirobifluorenyl, 1-naphthyl or 2-naphthyl, indole, benzofuran, benzothiophene, 1-carbazole, 2-carbazole, 3-carbazole or 4-carbazole, 1-dibenzofuran, 2-dibenzofuran, 3-dibenzofuran or 4-dibenzofuran, 1-dibenzothiophene, 2-dibenzothiophene, 3-dibenzothiophene or 4-dibenzothiophene, indolocarbazole, 2-pyridine, 3-pyridine or 4-pyridine, 2-pyrimidine, 4-pyrimidine or 5-pyrimidine, pyrazine, pyridazine, triazine, phenanthrene or terphenyl, each of which may be substituted by one or more R ¹ And (4) substituting the group. Most preferably, ar ² And Ar ³ Identical or different in each case and selected from the group consisting of benzene, biphenyl, in particular orthobiphenyl, metabiphenyl or para-biphenyl, terphenyl, in particular orthoterphenyl, metaterphenyl or para-terphenyl or branched-chain terphenyl, quaterphenyl, in particular orthoquaterphenyl, metaquaterphenyl or para-quaterphenyl or branched-chain quaterphenyl, fluorene, in particular 1-fluorene, 2-fluorene, 3-fluorene or 4-fluorene, or spirobifluorene, in particular 1-spirobifluorene, 2-spirobifluorene, 3-spirobifluorene or 4-spirobifluorene.

In another preferred embodiment of the invention, R ¹ Identical or different on each occurrence and selected from H, D, F, CN, a linear alkyl radical having from 1 to 10 carbon atoms or a branched or cyclic alkyl radical having from 3 to 10 carbon atoms, where the alkyl radical may be substituted in each case by one or more R ² Substituted by radicals, or having 6 to 24 aromatic ring atoms and may in each case be substituted by one or more R ² A group-substituted aromatic or heteroaromatic ring system. In a particular advantage of the inventionIn selected embodiments, R ¹ Are identical or different on each occurrence and are selected from H, straight-chain alkyl radicals having from 1 to 6 carbon atoms, in particular having from 1,2,3 or 4 carbon atoms, or branched or cyclic alkyl radicals having from 3 to 6 carbon atoms, where the alkyl radicals may be substituted by one or more R ⁵ Substituted, but preferably unsubstituted, or have 6 to 13 aromatic ring atoms and can be substituted in each case by one or more R ⁵ The radicals are substituted, but preferably unsubstituted, aromatic or heteroaromatic ring systems.

In another preferred embodiment of the invention, R ² In each case identical or different and is H, an alkyl radical having from 1 to 4 carbon atoms or an aryl radical having from 6 to 10 carbon atoms, which may be substituted by alkyl radicals having from 1 to 4 carbon atoms, but is preferably unsubstituted.

Meanwhile, in the compound of the present invention processed by vacuum evaporation, the alkyl group preferably has not more than 5 carbon atoms, more preferably not more than 4 carbon atoms, and most preferably not more than 1 carbon atom. For compounds which are processed from solution, suitable compounds are also those which are substituted by alkyl groups, in particular by branched alkyl groups having up to 10 carbon atoms, or by oligoarylene groups, for example ortho-terphenyl, meta-terphenyl or para-terphenyl or branched terphenyl or quaterphenyl groups.

It is also possible that: the compounds comprise exactly two or exactly three structures of the formulae (I), (IIa) to (IIk), (IIIa) to (IIIk), (IV-1) to (IV-20), (V-1) to (V-40), (VI-1) to (VI-40), (VII-1) to (VII-50) and/or (VIII-1) to (VIII-50), where preferably with Y ¹ 、X ¹ 、X ² 、X ³ One of the aromatic or heteroaromatic ring systems to which at least one of the groups is bound is shared by both structures.

In a preferred configuration, the compound is selected from compounds of formula (D-1), (D-2), (D3) or (D-4):

wherein L is ¹ The radicals are linking groups, preferably bonds or aromatic or heteroaromatic ring systems which have from 5 to 40, preferably from 5 to 30, aromatic ring atoms and may be substituted by one or more R groups, and the other symbols and indices used have the definitions given above, in particular for the formulae (I) and/or the formulae (V-1) to (V-40).

In another preferred embodiment of the present invention, L ¹ Is a bond or an aromatic or heteroaromatic ring system having from 5 to 14 aromatic or heteroaromatic ring atoms, preferably an aromatic ring system having from 6 to 12 carbon atoms, and may be interrupted by one or more R ¹ Substituted, but preferably unsubstituted, with R ¹ May have the definitions given above, especially for formula (I). More preferably, L ¹ Is an aromatic ring system having 6 to 10 aromatic ring atoms or a heteroaromatic ring system having 6 to 13 heteroaromatic ring atoms, each of which may be substituted by one or more R ² Substituted, but preferably unsubstituted, with R ² May have the definitions given above, especially for formula (I).

More preferably, the symbol L shown in formula (D4) in particular ¹ In particular identical or different on each occurrence and is a bond or an aryl or heteroaryl radical having from 5 to 24 ring atoms, preferably from 6 to 13 ring atoms, more preferably from 6 to 10 ring atoms, such that the aromatic or heteroaromatic groups of the aromatic or heteroaromatic ring system are bonded directly to the corresponding atoms of the further group, i.e. to the corresponding atoms of the further group via atoms of the aromatic or heteroaromatic group.

Further possible situations are: l represented by the formula (D4) ¹ The groups comprise aromatic ring systems having no more than two fused aromatic and/or heteroaromatic 6-membered rings, preferably aromatic ring systems which do not comprise any fused aromatic or heteroaromatic ring systems. Thus, the naphthyl structure is preferred over the anthracene structure. Furthermore, fluorenyl, spirobifluorenyl, dibenzofuranThe phenyl and/or dibenzothienyl structures are preferred over the naphthyl structures.

Particular preference is given to structures which are not fused, for example phenyl, biphenyl, terphenyl and/or quaterphenyl structures.

Suitable aromatic or heteroaromatic ring systems L ¹ Examples of (A) are selected from ortho-, meta-or para-phenylene, ortho-, meta-or para-biphenylene, terphenylene, especially branched terphenylene, quaterphenylene, especially branched quaterphenylene, fluorenylene, spirobifluorenylene, dibenzofuranylene, dibenzothiophenylene and carbazolyl groups, each of which may be substituted with one or more R ¹ The radicals are substituted, but preferably unsubstituted.

The above-described preferred embodiments can be combined with each other as desired within the limits defined in claim 1. In a particularly preferred embodiment of the invention, the above-mentioned preferred features are present simultaneously.

According to the embodiments detailed above, examples of preferred compounds are the compounds shown in the following table:

preferred embodiments of the compounds of the invention are specified in the examples, which compounds can be used alone or in combination with further compounds for all purposes of the invention.

The above-described preferred embodiments may be combined with each other as needed as long as the conditions specified in claim 1 are satisfied. In a particularly preferred embodiment of the invention, the above-described preferred embodiments apply simultaneously.

The compounds of the invention can in principle be prepared by various methods. However, the method described below has been found to be particularly suitable.

Thus, the present invention also provides a process for the preparation of the compounds of the invention, wherein the synthesis has Z ¹ Group or Z ² Group or Z ¹ 、Z ² Basic skeleton of a precursor of one of the radicals, and introduction of Y by aromatic nucleophilic substitution or coupling reactions ¹ 、Y ² At least one of the groups.

Comprising a compound having Z ¹ Group or Z ² Suitable compounds of the basic skeleton of the radicals are in many cases commercially available, and the starting compounds detailed in the examples can be obtained by known methods and are therefore taken as reference.

These compounds can be reacted with further compounds by known coupling reactions, the requirements for which are known to the person skilled in the art, and the detailed description in the examples assists the person skilled in the art in carrying out these reactions.

All particularly suitable and preferred coupling reactions leading to C-C bond formation and/or C-N bond formation are those according to BUCHWALD, SUZUKI, YAMAMOTO, STILLE, HECK, NEGISHI, SONOGASHIRA and HIYAYAMA. These reactions are well known and these examples will provide further guidance to those skilled in the art.

The principles of the preparation processes detailed above are in principle known from the literature on analogous compounds and can be readily used by the person skilled in the art for preparing the compounds of the invention. More information can be found in the examples.

By these methods, if necessary followed by purification, such as recrystallization or sublimation, high purity, preferably higher than 99%, can be obtained (by ¹ H NMR and/or HPLC).

The compounds of the invention may also be mixed with polymers. These compounds can likewise be incorporated covalently into polymers. This is particularly true for compounds substituted with a reactive leaving group such as bromo, iodo, chloro, boronate or boronate, or with a reactive polymerizable group such as alkene or oxetane. These can be used as monomers for the production of corresponding oligomers, dendrimers or polymers. The oligomerization or polymerization is preferably effected by halogen functionality or boronic acid functionality or by polymerizable groups. It is also possible to crosslink the polymers by means of such groups. The compounds and polymers of the invention may be used in the form of crosslinked or uncrosslinked layers.

The present invention therefore also provides an oligomer, polymer or dendrimer containing one or more of the structures of the formula (I) and the preferred embodiments of the formula or compounds of the invention as detailed above, in which there are present one or more bonds to the polymer, oligomer or dendrimer of the compounds of the invention or of the structures of the formula (I) and the preferred embodiments of the formula. According to the structure of formula (I) and preferred embodiments of this formula or the linkages of the compounds, these thus form side chains or linkages in the main chain of the oligomer or polymer. The polymer, oligomer or dendrimer may be conjugated, partially conjugated or non-conjugated. The oligomer or polymer may be linear, branched or dendritic. The same preferred features as described above apply to the oligomers, dendrimers and repeating units of the compounds of the invention in the polymer.

To prepare oligomers or polymers, the monomers of the invention are homopolymerized or copolymerized with additional monomers. The following copolymers are preferred: wherein the units of formula (I) or of the preferred embodiments listed above and below are present in the range from 0.01 to 99.9mol%, preferably from 5 to 90mol%, more preferably from 20 to 80 mol%. Suitable and preferred comonomers forming the basic backbone of the polymer are selected from fluorene (e.g. according to EP 842208 or WO 2000/022026), spirobifluorene (e.g. according to EP 707020, EP 894107 or WO 2006/061181), p-phenylene (e.g. according to WO 92/18552), carbazole (e.g. according to WO 2004/070772 or WO 2004/113468), thiophene (e.g. according to EP 1028136), dihydrophenanthrene (e.g. according to WO 2005/014689), cis-and trans-indenofluorene (e.g. according to WO 2004/041901 or WO 2004/113412), ketones (e.g. according to WO 2005/040302), phenanthrene (e.g. according to WO 2005/104264 or WO 2007/017066) or a plurality of these units. The polymers, oligomers and dendrimers may also contain further units, for example hole transport units, especially those based on triarylamines, and/or electron transport units.

Of particular interest are also the compounds of the invention which are characterized by a high glass transition temperature. In this connection, particular preference is given to compounds according to the invention having the structure of the formula (I) or the preferred embodiments listed above and below having a glass transition temperature, determined in accordance with DIN 51005 (version 2005-08), of at least 70 ℃, more preferably at least 110 ℃, even more preferably at least 125 ℃, particularly preferably at least 150 ℃.

For processing the compounds of the invention from the liquid phase, for example by spin coating or by printing methods, formulations of the compounds of the invention are required. These formulations may be, for example, solutions, dispersions or emulsions. For this purpose, a mixture of two or more solvents can be preferably used. Suitable and preferred solvents are, for example, toluene, anisole, o-, m-or p-xylene, methyl benzoate, mesitylene, tetralin, o-dimethoxybenzene, THF, methyl-THF, THP, chlorobenzene, bis-chlorobenzene

Alkanes, phenoxytoluene, especially 3-phenoxytoluene, (-) -fenchytone, 1,2,3,5-tetramethylbenzene, 1,2,4,5-tetramethylbenzene, 1-methylnaphthalene, 2-methylbenzothiazole, 2-phenoxyethanol, 2-pyrrolidone, 3-methylanisole, 4-methylanisole, 3,4-dimethylanisole, 3,5-dimethylanisole, acetophenone, α -terpineol, benzothiazole, butyl benzoate, cumene, cyclohexanol, cyclohexanone, cyclohexylbenzene, decalin, dodecylbenzene, ethyl benzoate, indane, NMP, p-cymene, phenetole, 1,4-diisopropylbenzene, dibenzyl ether, diethylene glycol butyl methyl ether, triethylene glycol butyl ether, diethylene glycol butyl ether, triethylene glycol dimethyl ether, diethylene glycol monobutyl ether, tripropylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, 2-naphtalene, pentylbenzene, hexylbenzene, heptylbenzene, octylbenzene, tetraethylene glycol dimethyl etherBenzene, 1,1-bis (3,4-dimethylphenyl) ethane, 2-methylbiphenyl, 3-methylbiphenyl, 1-methylnaphthalene, 1-ethylnaphthalene, ethyl octanoate, diethyl sebacate, octyl octanoate, heptylbenzene, menthyl isovalerate, cyclohexyl hexanoate or mixtures of these solvents.

Accordingly, the present invention also provides a formulation or composition comprising at least one compound of the invention and at least one additional compound. The further compound may, for example, be a solvent, in particular one of the abovementioned solvents or a mixture of these solvents. If the additional compound comprises a solvent, the mixture is referred to herein as a formulation. The further compound may alternatively be at least one other organic or inorganic compound, which is also used in electronic devices, for example a light emitter and/or a matrix material, wherein these compounds are different from the compounds of the invention. Suitable emitters and matrix materials are listed below in connection with organic electroluminescent devices. These additional compounds may also be polymeric.

Accordingly, the present invention also provides a composition comprising a compound of the invention and at least one additional organic functional material. The functional material is typically an organic or inorganic material introduced between the anode and the cathode. Preferably, the organic functional material is selected from fluorescent emitters, phosphorescent emitters, emitters exhibiting TADF (thermally activated delayed fluorescence), host materials, electron transport materials, electron injection materials, hole conducting materials, hole injection materials, electron blocking materials, hole blocking materials, wide band gap materials and n-type dopants.

The invention also provides the use of the compounds according to the invention in electronic devices, in particular in organic electroluminescent devices, preferably as emitters, more preferably as green, red or blue emitters. In this case, the compounds of the invention preferably exhibit fluorescent properties and therefore preferentially provide fluorescent emitters. Furthermore, the compounds of the present invention may be used as host materials, electron transport materials and/or hole conductor materials. Z can be used particularly advantageously here ¹ 、Z ² 、Z ³ 、Z ⁴ Compounds of the invention in which a number of, preferably all, of the radicals are N are useful as hole-conducting materials. Z is also particularly advantageously used ¹ 、Z ² 、Z ³ 、Z ⁴ The compounds of the invention in which many, preferably all, of the groups are B are useful as electron transport materials.

The present invention additionally provides an electronic device comprising at least one compound according to the invention. In the context of the present invention, an electronic device is a device comprising at least one layer, said at least one layer comprising at least one organic compound. The component may also comprise an inorganic material or a layer formed entirely of an inorganic material.

The electronic device is preferably selected from the group consisting of organic electroluminescent devices (OLED, sOLED, PLED, LEC, etc.), preferably Organic Light Emitting Diodes (OLED), small molecule based organic light emitting diodes (sOLED), polymer based organic light emitting diodes (PLED), light emitting electrochemical cells (LEC), organic laser diodes (O-laser), organic plasma light emitting devices (d.m.koller et al, nature Photonics 2008,1-4), organic integrated circuits (O-IC), organic field effect transistors (O-FET), organic thin film transistors (O-TFT), organic light emitting transistors (O-LET), organic solar cells (O-SC), organic optical detectors, organic photoreceptors, organic field quenching devices (O-FQD) and organic electric sensors, preferably organic electroluminescent devices (OLED, sOLED, PLED, LEC, etc.), more preferably Organic Light Emitting Diodes (OLED), small molecule based organic light emitting diodes (sOLED), polymer based organic light emitting diodes (PLED), in particular phosphorescent diodes.

The organic electroluminescent device includes a cathode, an anode, and at least one light-emitting layer. In addition to these layers, it may also comprise further layers, for example in each case one or more hole-injecting layers, hole-transporting layers, hole-blocking layers, electron-transporting layers, electron-injecting layers, exciton-blocking layers, electron-blocking layers and/or charge-generating layers. An intermediate layer having an exciton-blocking function may also be introduced between the two light-emitting layers. However, it should be noted that each of these layers does not necessarily have to be present. In this case, the organic electroluminescent device may have one light-emitting layer, or may have a plurality of light-emitting layers. If there are a plurality of light-emitting layers, these preferably have a plurality of emission peaks between 380nm and 750nm in total, so that the overall result is a white light emission; in other words, a plurality of light-emitting compounds which can emit fluorescence or phosphorescence are used in the light-emitting layer. Particularly preferred are systems with three light-emitting layers, wherein the three layers exhibit blue, green and orange or red light emission. The organic electroluminescent device of the invention can also be a tandem electroluminescent device, in particular a white-emitting OLED.

Depending on the exact structure, the compounds of the invention can be used in different layers. Preference is given to organic electroluminescent devices which comprise, as emitters, preferably red, green or blue emitters, in the light-emitting layer, compounds of the formula (I) or compounds of the preferred embodiments detailed above.

When the compounds of the invention are used as emitters in the light-emitting layer, preference is given to using known suitable matrix materials.

Preferred mixtures of the compounds of the invention and the matrix material contain between 99% and 1% by volume, preferably between 98% and 10% by volume, more preferably between 97% and 60% by volume, in particular between 95% and 80% by volume, of matrix material, based on the total mixture of emitter and matrix material. Accordingly, the mixture contains between 1% and 99% by volume, preferably between 2% and 90% by volume, more preferably between 3% and 40% by volume, in particular between 5% and 20% by volume of luminophores, based on the total mixture of luminophores and matrix material.

Suitable matrix materials which can be used in combination with the compounds of the invention are aromatic ketones, aromatic phosphine oxides or aromatic sulfoxides or sulfones (for example according to WO 2004/013080, WO 2004/093207, WO 2006/005627 or WO 2010/006680); triarylamines, carbazole derivatives, such as CBP (N, N-biscarbazolylbiphenyl) or carbazole derivatives (disclosed in WO 2005/039246, US 2005/0069729, JP 2004/288381, EP 1205527, WO 2008/086851 or WO 2013/041176); indolocarbazole derivatives (e.g. according to WO 2007/063754 or WO 2008/056746); indenocarbazole derivatives (e.g. according to WO 2010/136109, WO 2011/000455, WO 2013/041176 or WO 2013/056776); azacarbazole derivatives (e.g. according to EP 1617710, EP 1617711, EP 1731584, JP 2005/347160); bipolar matrix materials (e.g. according to WO 2007/137725); silanes (e.g. according to WO 2005/111172), boron nitrogen heterocycles or borates (e.g. according to WO 2006/117052); triazine derivatives (e.g. according to WO 2007/063754, WO 2008/056746, WO 2010/015306, WO 2011/057706, WO 2011/060859 or WO 2011/060877), zinc complexes (e.g. according to EP 652273 or WO 2009/062578); silicon-diazacyclo-slow or silicon-tetraazazepine-slow derivatives (according to WO 2010/054729); phosphorus diazacyclo-slow derivatives (e.g. according to WO 2010/054730); bridged carbazole derivatives (e.g. of WO 2011/042107, WO 2011/060867, WO 2011/088877 and WO 2012/143080), terphenyl fork derivatives (e.g. according to WO 2012/048781); dibenzofuran derivatives (e.g. according to WO 2015/16942, WO 2016/015810, WO 2016/023608, WO 2017/148564 or WO 2017/148565) or dicarbazoles (e.g. according to JP 3139321 B2).

Furthermore, the co-host used may be a compound which does not participate to a significant extent even if it participates in the extent of charge transport, as described in, for example, WO 2010/108579. Particularly suitable as co-matrix material in combination with the compounds of the invention are compounds which have a large band gap and which themselves do not participate at least to a significant extent even in the charge transport of the light-emitting layer. Such materials are preferably pure hydrocarbons. Examples of such materials can be found in, for example, WO 2009/124627 or WO 2010/006680.

In a preferred configuration, the compounds according to the invention used as emitters are preferably used in combination with one or more phosphorescent materials (triplet emitters) and/or compounds as TADF (thermally activated delayed fluorescence) host materials. Here, preference is given to forming superfluorescent and/or hyperphosphorescent systems.

WO 2015/091716 A1 and WO 2016/193243 A1 disclose OLEDs which contain phosphorescent compounds and fluorescent emitters in the light-emitting layer, wherein energy is transferred from the phosphorescent compounds to the fluorescent emitters (hyperphosphorescence). In this case, the phosphorescent compound behaves correspondingly as a host material. As is known to those skilled in the art, host materials have higher singlet and triplet energies than emitters, so that energy from the host material can also be transferred to the emitter with maximum efficiency. The systems disclosed in the prior art have exactly such an energy relationship.

In the context of the present invention, phosphorescence is understood to mean light emission from an excited state with a higher spin multiplicities, i.e. a spin state >1, in particular light emission from an excited triplet state. In the context of the present application, all luminescent complexes with transition metals or lanthanides, in particular all iridium, platinum and copper complexes, should be regarded as phosphorescent compounds.

Suitable phosphorescent light-emitting compounds (= triplet emitters) are in particular those which: which upon suitable excitation emits light, preferably in the visible region, and also contains at least one atom having an atomic number greater than 20, preferably greater than 38 and less than 84, more preferably greater than 56 and less than 80, especially a metal having such an atomic number. Preferred as phosphorescent emitters are compounds containing copper, molybdenum, tungsten, rhenium, ruthenium, osmium, rhodium, iridium, palladium, platinum, silver, gold or europium, in particular iridium or platinum-containing compounds.

Examples of such emitters can be found in the following applications: WO 00/70655, WO 2001/41512, WO 2002/02714, WO 2002/15645, EP 1191613, EP 1191612, EP 1191614, WO 05/033244, WO 05/019373, US 2005/0258742, WO 2009/146770, WO 2010/015307, WO 2010/031485, WO 2010/054731, WO 2010/054728, WO 2010/086089, WO 2010/099852, WO 2010/102709, WO 2011/032626, WO 2011/066898, WO 2011/157339, WO 2012/007086, WO 2014/008982, WO 2014/023377, WO 2011 WO 2014/094961, WO 2014/094960, WO 2015/036074, WO 2015/104045, WO 2015/117718, WO 2016/015815, WO 2016/124304, WO 2017/032439, WO 2018/011186, WO 2018/001990, WO 2018/019687, WO 2018/019688, WO 2018/041769, WO 2018/054798, WO 2018/069196, WO 2018/069197, WO 2018/920673, WO 2018/178001, WO 2018/177981, WO 2019/020538, WO 2019/115423, WO 2019/158453 and WO 2019/179909. In general, all phosphorescent complexes used in phosphorescent electroluminescent devices according to the prior art and known to the person skilled in the art in the field of organic electroluminescence are suitable and the person skilled in the art is able to use further phosphorescent complexes without inventive effort.

As set out above, the compounds of the present invention may preferably be used in combination with a TADF host material and/or a TADF emitter.

For example, b.h. uoyama et al, nature 2012, 492, 234 describes a method known as Thermally Activated Delayed Fluorescence (TADF). To implement this method, less than about 2000cm, for example, is required in the luminaire ^-1 Of (2) a relatively small singlet-triplet splitting Δ E (S) ₁ –T ₁ ). To generate T which is spin-forbidden in principle ₁ —→S ₁ Transitions, and luminophores, other compounds with strong spin-orbit coupling can be provided in the matrix, such that intersystem crossing is achieved by spatial proximity and thus interactions between molecules, or spin-orbit coupling is generated by metal atoms present in the luminophores.

In another embodiment of the present invention, the organic electroluminescent device of the present invention does not contain any separate hole injection layer and/or hole transport layer and/or hole blocking layer and/or electron transport layer, which means that the light-emitting layer is directly adjacent to the hole injection layer or anode and/or the light-emitting layer is directly adjacent to the electron transport layer or electron injection layer or cathode, as described in, for example, WO 2005/053051. Furthermore, a metal complex which is the same as or similar to the metal complex in the light-emitting layer may be used as a hole transporting or hole injecting material directly adjacent to the light-emitting layer, as described in, for example, WO 2009/030981.

Also preferred are organic electroluminescent devices which comprise compounds of the formula (I) or the preferred embodiments detailed above as hole conductor material in the hole-conducting layer. Particular preference is given here to Z ¹ And Z ² At least one, preferably two, of the radicals are N, and Y ¹ And Y ² At least one, preferably two, of the groups are N (Ar), N (R), P (Ar), P (R), O, S or Se, preferably N (Ar), N (R), O or S, more preferably N (Ar). Furthermore, Z is particularly preferred here ¹ 、Z ² Radical ofIs N and Z ³ 、Z ⁴ Compounds in which at least one, preferably two, of the radicals are N.

Also preferred are organic electroluminescent devices comprising compounds of the formula (I) or the preferred embodiments detailed above as electron transport material in the electron conducting layer. Particularly preferred here is Z ¹ And Z ² At least one, preferably two of the radicals are B and Z ³ And Z ⁴ At least one, preferably two, of the radicals are B. Furthermore, particular preference is given here to compounds in which Z is ¹ 、Z ² At least one, preferably two of the radicals are B and Z ³ 、Z ⁴ Compounds in which at least one, preferably two, of the radicals are B.

In the further layers of the organic electroluminescent device of the invention, any material commonly used in the art may be used. The person skilled in the art is therefore able, without inventive effort, to combine any material known for use in organic electroluminescent devices with the compounds of the formula (I) according to the invention or the preferred embodiments listed above.

Also preferred is an organic electroluminescent device characterized in that one or more layers are coated by a sublimation process. In this case, less than 10% by vacuum sublimation system ^-5 Mbar, preferably less than 10 ^-6 The material was applied by vapor deposition at an initial pressure of mbar. However, the initial pressure may also be even lower, e.g. below 10 ^-7 Millibar.

Also preferred is an organic electroluminescent device characterized in that one or more layers are coated by the OVPD (organic vapor deposition) method or sublimation with a carrier gas. In this case, 10 ^-5 The material is applied at a pressure between mbar and 1 bar. A special example of such a method is the OVJP (organic vapor jet printing) method, in which the material is applied directly through a nozzle and is thus structured.

Also preferred is an organic electroluminescent device, characterized in that one or more layers are produced from a solution, for example by spin coating, or by any printing method, for example screen printing, flexography, offset printing, LITI (photo induced thermal imaging, thermal transfer), inkjet printing or nozzle printing. For this purpose, soluble compounds are required, for example, which are obtained by suitable substitution.

The formulations for applying the compounds of formula (I) or the preferred embodiments thereof described above are novel. The present invention therefore also provides a formulation comprising at least one solvent and a compound according to formula (I) or a compound of preferred embodiments thereof as detailed above.

Furthermore, a hybrid process is possible, in which, for example, one or more layers are applied from solution and one or more further layers are applied by vapor deposition.

These methods are generally known to those skilled in the art and can be applied without inventive step to organic electroluminescent devices comprising the compounds according to the invention.

The compounds according to the invention and the organic electroluminescent devices according to the invention have the particular feature of improved lifetime compared to the prior art. At the same time, further electronic properties of the electroluminescent device, such as efficiency or operating voltage, remain at least as good. In a further variant, the compounds according to the invention and the organic electroluminescent devices according to the invention have, in particular, improved efficiency and/or operating voltage and a higher lifetime than the prior art.

Compared to the prior art, the electronic device of the invention, in particular the organic electroluminescent device, is notable for one or more of the following surprising advantages:

1. electronic devices, in particular organic electroluminescent devices, which comprise as emitter compounds of the formula (I) or preferred embodiments described above and below have a very narrow emission band with a very low Full Width Half Maximum (FWHM) value and lead to particularly pure color emissions which can be recognized by low CIE y values. It is particularly surprising here that blue emitters with low FWHM values and emitters with low FWHM which emit in the green, yellow or red region of the color spectrum are provided.

2. Electronic devices, in particular organic electroluminescent devices, which comprise the compounds of the formula (I) or preferred embodiments described above and below, in particular as emitters, as hole conductor materials and/or as electron transport materials, have very good lifetimes. In this case, these compounds lead in particular to a low roll-off, i.e. the power efficiency of the device at high luminance decreases by a small amount.

3. Electronic devices, in particular organic electroluminescent devices, comprising compounds of the formula (I) or preferred embodiments described above and below as emitters, as hole-conducting materials and/or electron-transporting materials have excellent efficiency. In this case, the compounds according to the invention having the structure or preferred embodiments of the formula (I) described above and below lead to a low operating voltage when used in electronic devices.

4. The compounds of formula (I) or preferred embodiments described above and below according to the invention exhibit a very high stability and lifetime.

5. With the compounds of formula (I) or preferred embodiments described above and below, the formation of optical loss channels in electronic devices, especially organic electroluminescent devices, can be avoided. These devices are therefore characterized by a high PL efficiency and hence a high EL efficiency of the emitter, and by an excellent energy transfer from the host to the dopant.

6. The compounds of formula (I) or preferred embodiments described above and below have excellent glass film formation.

7. The compounds of formula (I) or preferred embodiments described above and below form very good films from solution and show excellent solubility.

These above-mentioned advantages are not accompanied by too high a deterioration of other electronic properties.

It should be noted that variations of the described embodiments of the invention are covered by the scope of the invention. Any features disclosed in this specification may be interchanged with alternative features serving the same purpose or an equivalent or similar purpose unless expressly excluded. Thus, unless stated otherwise, any feature disclosed in this disclosure should be considered a generic series of embodiments or as an equivalent or similar feature.

All of the features of the present invention may be combined with each other in any manner, unless the specific features and/or steps are mutually exclusive. This is particularly true of the preferred features of the present invention. Likewise, features that are not necessarily combined may be used separately (rather than in combination).

Furthermore, it should be noted that many of the features, and in particular those of the preferred embodiments of the present invention, should be considered inventive in their own right and not just as embodiments of the present invention. Independent protection may be sought for these features in addition to or in lieu of any presently claimed invention.

The teachings of the present disclosure may be extracted and combined with other embodiments.

The present invention is illustrated in detail by the following examples, which are not intended to be limiting thereby. Those skilled in the art will be able to practice the invention within the full scope of the disclosure using the information given without inventive step, and to prepare other compounds of the invention and use them in electronic devices or to employ the methods of the invention without inventive step.

Example (b):

unless otherwise stated, the following syntheses are carried out in anhydrous solvents under a protective gas atmosphere. The metal complexes are furthermore treated in the dark or under yellow light. Solvents and reagents are available, for example, from Sigma-ALDRICH or ABCR. The corresponding numbers in brackets or quoted numbers for individual compounds refer to the CAS number of the compounds known from the literature. Where a compound may have multiple enantiomeric, diastereomeric or tautomeric forms, one form is shown in a representative manner.

Synthesis of synthon S:

example S1:

similar to the procedure in Chung-Chieh Lee et al, synthesis 2008,9, 1359. The complete procedure includes treatment under protective gas.

34.0g (120 mmol) of 1-bromo-2-iodobenzene [583-55-1]8.5g (50 mmol) 2,3-dihydro-1H-piperidine [69098-80-2]20.7g (150 mmol) of potassium carbonate and 1.9g (10 mmol) of copper iodide [7681-65-4 ]]2.9g (20 mmol) of 1R,2R-N, N-dimethylcyclohexane-1,2-diamine [67579-81-8 ]]A mixture of 50g of glass beads and 200ml of o-xylene was stirred at 130 ℃ for 24h. After cooling, 300ml of ethyl acetate and 500ml of water were added to the reaction mixture, the organic phase was removed, washed once with 500ml of water and twice with 300ml each of saturated sodium chloride solution and dried over magnesium sulfate. The mixture is filtered through a bed of silica gel in the form of an ethyl acetate slurry, the filtrate is concentrated to dryness, the residue is boiled with 150ml of ethanol, the solid is filtered off with suction, washed twice with 30ml of ethanol, dried under reduced pressure and recrystallized from acetonitrile/DCM (dichloromethane). Further purification can be achieved by flash chromatography on an automated column system (Torrent, from a.semrau). Yield: 15.8g (33 mmol) 65%; by passing ¹ The purity was about 95% by H NMR.

The following compounds can be prepared in a similar manner:

example, dopant D1:

the following sequence of steps 1 to 3 was carried out as a three-stage one-pot reaction. The treatment in step 3 is performed under a protective gas.

The first step is as follows: lithiation of S1:

intermediate, not isolated

A baked, argon-inerted, four-necked flask with magnetic stir bar, dropping funnel, water separator, reflux condenser and argon blanket was charged with 24.0g (50 mmol) of S1 dissolved in 1700ml of tert-butylbenzene. The reaction mixture is cooled to-40 ℃ and 110.5ml (210 mmol) of a 1.9 molar solution of tert-butyllithium in n-pentane are then added dropwise. The mixture was stirred at-40 ℃ for a further 30 minutes, allowed to warm to room temperature and then heated to 70 ℃ during which time the n-pentane was distilled off over a water separator in about 1 hour.

Step 2: transmetallation and cyclization

Intermediate, not isolated

The reaction mixture was cooled back to-40 ℃. 10.4ml (110 mmol) of boron tribromide are added dropwise over a period of about 10 minutes. After the addition was complete, the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was then cooled to 0 ℃ and 19.2ml (110 mmol) of diisopropylethylamine were added dropwise over a period of about 30 minutes. The reaction mixture was then stirred at 160 ℃ for 16 hours. After cooling, the diisopropylethylamine hydrobromide was filtered off using a double frit and the filtrate was cooled to-78 deg.C

And step 3: arylation of

Intermediate, not isolated

A second, baked, argon-inerted Schlenk flask with a magnetic stir bar was charged with 27.8g (150 mmol) of 2-bromo-1,3-xylene [576-22-7 ] dissolved in 1000mL of diethyl ether]And cooled to-78 deg.C, then 60.0ml (150 mmol) of n-butyllithium in 2.5M n-hexane was added dropwise thereto, and the mixture was stirred for further 30 minutes. The reaction mixture was allowed to warm to room temperature, stirred for an additional 1 hour and the solvent was completely removed under reduced pressure. The organolithium was suspended in 300ml of toluene and transferred to the low temperature reaction mixture from step 2. The mixture was stirred for another 1 hour, and the reaction mixture was allowed to stand to warm to room temperature overnight. To the reaction mixture was carefully added 15ml of acetone and concentrated to dryness. The oily residue was taken up with DCM

And filtered hot through a silica bed together with the n-pentane-DCM mixture (10. The filtrate was concentrated to dryness. The residue was subjected to two flash chromatographies (silica gel, n-heptane/ethyl acetate, torrent automated column system from a.semrau).

The method comprises the following steps: by oxidation to D1

Similar to the procedure in R.Doringer et al, monatshefte fur Chemie,2006,137,185. The product from step 3 was dissolved in 150ml of chlorobenzene, 20g of activated 3A molecular sieve were added and the mixture was stirred at 60 ℃ in the dark in air until the oxidation was complete (about 5 h). The molecular sieve is filtered off, rinsed with a little chlorobenzene and the mixture is concentrated to dryness under reduced pressure. The residue was subjected to two flash chromatographies (silica gel, n-heptane/ethyl acetate, torent automated column system from a. Semrau). Further purification was achieved by repeated thermal extraction crystallization with DCM/acetonitrile and final fractional sublimation or heat treatment under reduced pressure. Yield: 12.43g (22 mmol) 44%; by passing ¹ The purity was about 99.9% by H NMR.

The following compounds can be prepared analogously:

examples, dopants D6PA, D6PB and D6PC

Prepared from D6 by flash vacuum pyrolysis, carrier gas: argon, reduced pressure about 10 ^-2 Torr, pyrolysis zone temperature 550 ℃, catalyst: 1% pdo on alumina. Chromatography, DCM/n-heptane, silica gel. Yield: D100A 9%; D100B 15%, and D100C 8%.

Production of OLED components

1) Vacuum-processed parts:

the OLEDs of the invention and of the OLEDs according to the prior art are manufactured by the general method according to WO 2004/058911, which is adapted to the situation described here (layer thickness variation, materials used).

In the following examples, the results of various OLEDs are presented. Clean glass plates coated with structured ITO (indium tin oxide) with a thickness of 50nm (cleaned in a Miele laboratory glass washer, merck Extran cleaner) were pretreated with UV ozone for 25 minutes (PR-100 UV ozone generator from UVP) and, within 30 minutes, for improved processing, 20nm of PEDOT: PSS (poly (3,4-ethylenedioxythiophene) poly (styrenesulfonate) was coated as CLEVIOS ^TM P VP AI 4083 from Heraeus Precious Metals GmbH Deutschland, spin coated from aqueous solution) and baked at 180 ℃ for 10 minutes. These coated glass plates form the substrate to which the OLED is applied.

OLEDs have essentially the following layer structure: substrate/hole injection layer 1 (HIL 1) consisting of Ref-HTM1 (available from Novaled) doped with 5% ndp-9, 20 nm/hole transport layer 1 (HTL 1) comprising: 150nm HTM1 for UV and blue OLEDs; 50nm for green and yellow OLEDs; the 110nm for red OLED/hole transport layer 2 (HTL 2) comprises: 10nm for blue OLEDs; 20nm for green and yellow OLEDs; 10nm for red OLED/emitting layer (EML): 25nm for blue OLEDs; 40nm for green and yellow OLEDs; 35nm for red OLEDs/Hole Blocking Layer (HBL) 10 nm/Electron Transport Layer (ETL) 30 nm/Electron Injection Layer (EIL) comprises 1nm ETM2/and finally a cathode. The cathode is formed of an aluminum layer having a thickness of 100 nm.

First, a vacuum processed OLED is described. For this purpose, all materials are applied by thermal vapor deposition in a vacuum chamber. In this case, the light-emitting layer always consists of at least one host material (host material) and a light-emitting dopant (emitter) which is added to the host material(s) in a specific volume proportion by co-evaporation. The details given in this form of SMB1: D1 (95%) mean here that the material SEB1 is present in the layer in a proportion by volume of 95% and D1 is present in the layer in a proportion of 5%. Similarly, the electron transport layer may also be composed of a mixture of two materials. The exact structure of the OLED can be seen in table 1. The materials used to produce the OLEDs are shown in table 3.

OLEDs are characterized in a standard manner. For this purpose, the electroluminescence spectrum, from a current-voltage-luminous density characteristic (IUL characteristic) exhibiting a lambertian luminous characteristic, calculates a current efficiency (measured in cd/a), a power efficiency (measured in lm/W), and an external quantum efficiency (EQE, measured in percentage) as a function of luminous density. At 1000cd/m ² Recording the electroluminescence spectra, which are used to infer the luminescence color and EL-FWHM value (electroluminescence-full width at half maximum-EL, i.e. the spectral width of the EL luminescence at half the peak height, in eV; for better comparability over the whole spectral range).

Use of the compounds of the invention as materials in OLEDs:

one use of the compounds of the invention can be as dopants in the light-emitting layer and as transport or barrier materials (HBLs) in OLEDs. Compound D-ref.1 according to table 3 was used as a comparison according to the prior art. The results of the OLEDs are collated in table 2.

Table 1: structure of OLED

Table 2: results of vacuum processed OLEDs

2) Solution processing of the parts:

the production of solution-based OLEDs is described essentially in documents such as WO 2004/037887 and WO 2010/097155. The following examples combine the two production methods (application from the gas phase and processing from solution) such that the layers up to and including the light-emitting layer are processed from solution and the subsequent layers (hole-blocking layer/electron-transporting layer) are applied by vapor deposition under reduced pressure. For this purpose, the general methods described above are adapted to the cases described here (layer thickness variation, material) and combined as follows.

The configuration used is therefore as follows:

-a substrate,

-ITO(50nm)，

-PEDOT(20nm)，

-a hole transport layer (HIL 2) (20 nm),

a light emitting layer (92% host, 8% dopant) (60 nm),

an electron transport layer (ETM 1% 50 + ETM 2% 50%) (20 nm),

-a cathode (aluminium).

The substrate used was a glass plate coated with structured ITO (indium tin oxide) with a thickness of 50 nm. For better processing, it is coated with buffer (PEDOT) Clevios P VP AI 4083 (Heraeus Clevios GmbH, leverkusen); PEDOT is uppermost. Spin coating was performed from water under air. The layer was then baked at 180 ℃ for 10 minutes. A hole-transporting layer and a light-emitting layer are applied to the glass plate thus coated. The hole transport layer was a polymer of the structure shown in table 3, which was synthesized according to WO 2010/097155. The polymer is dissolved in toluene so that the solution generally has a solids content of about 5g/l, in which case, as is the case here, a layer thickness of typically 20nm of the device will be obtained by spin coating. These layers were spin coated in an inert gas atmosphere (argon in this case) and baked at 180 ℃ for 60 minutes.

The light-emitting layer always comprises at least one host material (host material) and a light-emitting dopant (emitter). The details given in the form such as H1 (92%): D (8%) here mean that the material H1 is present in the light-emitting layer in a proportion by weight of 92% and the dopant D is present in the light-emitting layer in a proportion by weight of 8%. The mixture for the light-emitting layer was dissolved in toluene or chlorobenzene. A typical solids content of this solution is about 18g/l, at which point a typical layer thickness of 60nm of the device will be achieved by spin coating as is the case here. The layers were spin coated in an inert gas atmosphere (argon in this case) and baked at 140 to 160 ℃ for 10 minutes. The materials used are shown in table 3.

The materials for the electron transport layer and for the cathode are applied by thermal vapor deposition in a vacuum chamber. For example, the electron transport layer may be composed of more than one material, which are added to each other in a specific volume ratio by co-evaporation. Details given in the form such as ETM1: ETM2 (50%: 50%) here mean that ETM1 and ETM2 materials are present in the layer in a volume proportion of 50% each. The materials used in this case are shown in table 3.

Table 2: at 1000cd/m ² Results of lower solution processing of OLEDs

Table 3: structural formula of material used

Some of the compounds of the invention show a narrower or relatively narrower electroluminescence spectrum compared to the reference, identifiable by a smaller or equal EL-FWHM value (electroluminescence-full width at half maximum-width of the EL luminescence spectrum at half the peak height in eV). A narrower electroluminescence spectrum leads to a significant improvement in color purity (lower CIE y values). Furthermore, the EQE value (external quantum efficiency) is significantly larger and the operating voltage is lower than the reference, which results in a significant improvement in the power efficiency of the device, thereby reducing power consumption.

Claims

1. A compound comprising at least one structure of formula (I),

the symbols and subscripts used therein are as follows:

Z ¹ 、Z ² in each case identical or different and is N or B;

W ¹ 、W ² 、W ³ 、W ⁴ in each case identical or different and is either CAr, X, or two adjacent W ¹ 、W ² 、W ³ 、W ⁴ The group is Ar;

Y ¹ identical or different in each case and are N (Ar), N (R), P (Ar), P (R), P (= O) Ar, P (= O) R, P (= S) Ar, P (= S) R, B (Ar), B (R), al (Ar), al (R), ga (Ar), ga (R), C = O, C (R) ₂ 、Si(R) ₂ 、C＝NR、C＝NAr、C＝C(R) ₂ O, S, se, S = O or SO ₂ ；

Y ² Identical or different in each case and is a bond, N (Ar), N (R), P (Ar), P (R), P (= O) Ar, P (= O) R, P (= S) Ar, P (= S) R, B (Ar), B (R), al (Ar), al (R), ga (Ar), ga (R), C = O, C (R) ₂ 、Si(R) ₂ 、C＝NR、C＝NAr、C＝C(R) ₂ O, S, se, S = O or SO ₂ ；

x is identical or different on each occurrence and is N or CR, with the proviso that X, X is in one ring ³ No more than two of the groups are N;

X ¹ in each case the same or different, and is N, CR ^a Or CAr, provided that X is in a ring ¹ 、X ² 、X ³ No more than two of the groups are N;

X ² in each case identical or different and is N, CR ^b Or CAr, provided that X is in a ring ¹ 、X ² 、X ³ No more than two of the groups are N;

X ³ in each case identical or different and is N, CR ^c CAr, or X if p is 1 ³ Is C, provided that in one ring X, X ¹ 、X ² 、X ³ No more than two of the groups are N;

p is identical or different and is 0 or 1, where if W ³ 、W ⁴ Not Ar, p =1;

R、R ^a 、R ^b 、R ^c in each case identical or different and are H, D, OH, F, cl, br, I, CN, NO ₂ ，N(Ar') ₂ ，N(R ¹ ) ₂ ，C(＝O)OAr'，C(＝O)OR ¹ ，C(＝O)N(Ar') ₂ ，C(＝O)N(R ¹ ) ₂ ，C(Ar') ₃ ，C(R ¹ ) ₃ ，Si(Ar') ₃ ，Si(R ¹ ) ₃ ，B(Ar') ₂ ，B(R ¹ ) ₂ ，C(＝O)Ar'，C(＝O)R ¹ ，P(＝O)(Ar') ₂ ，P(＝O)(R ¹ ) ₂ ，P(Ar') ₂ ，P(R ¹ ) ₂ ，S(＝O)Ar'，S(＝O)R ¹ ，S(＝O) ₂ Ar'，S(＝O) ₂ R ¹ ，OSO ₂ Ar'，OSO ₂ R ¹ Straight-chain alkyl, alkoxy or thioalkoxy groups having from 1 to 40 carbon atoms or alkenyl or alkynyl groups having from 2 to 40 carbon atoms or branched or cyclic alkyl, alkoxy or thioalkoxy groups having from 3 to 20 carbon atoms, where the alkyl, alkoxy, thioalkoxy, alkenyl or alkynyl groups can in each case be substituted by one or more R ¹ Radical substitution of one or more non-adjacent CH ₂ The group can be represented by R ¹ C＝CR ¹ 、C≡C、Si(R ¹ ) ₂ 、C＝O、C＝S、C＝Se、C＝NR ¹ 、-C(＝O)O-、-C(＝O)NR ¹ -、NR ¹ 、P(＝O)(R ¹ ) -O-, -S-, SO or SO ₂ Instead of, or with 5 to 60 aromatic ring atoms and may in each case be substituted by one or more R ¹ Aromatic or heteroaromatic ring systems substituted by radicals, or having 5 to 60 aromatic ring atoms and which may be substituted by one or more R ¹ A group-substituted aryloxy or heteroaryloxy group; simultaneously, two R, R ^a 、R ^b 、R ^c The radicals may also form a ring system together or with further radicals;

ar' is identical or different on each occurrence and is an aromatic ring having 5 to 60 aromatic ring atoms and may be substituted by one or more R ¹ A group-substituted aromatic or heteroaromatic ring system; at the same time, the two Ar' groups bonded to the same carbon, silicon, nitrogen, phosphorus or boron atom may also be linked via a bridging group by a single bond or be selected from B (R) ¹ )、C(R ¹ ) ₂ 、Si(R ¹ ) ₂ 、C＝O、C＝NR ¹ 、C＝C(R ¹ ) ₂ 、O、S、S＝O、SO ₂ 、N(R ¹ )、P(R ¹ ) And P (= O) R ¹ Are linked together;

R ¹ in each case identical or different and are H, D, F, cl, br, I, CN, NO ₂ ，N(Ar”) ₂ ，N(R ² ) ₂ ，C(＝O)OAr”，C(＝O)OR ² ，C(＝O)Ar”，C(＝O)R ² ，P(＝O)(Ar”) ₂ ，P(Ar”) ₂ ，B(Ar”) ₂ ，B(R ² ) ₂ ，C(Ar”) ₃ ，C(R ² ) ₃ ，Si(Ar”) ₃ ，Si(R ² ) ₃ A linear alkyl, alkoxy or thioalkoxy group having from 1 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having from 3 to 40 carbon atoms or an alkenyl group having from 2 to 40 carbon atoms, each of which may be substituted by one or more R ² Substituted by radicals in which one or more non-adjacent CH ₂ The radical may be represented by-R ² C＝CR ² -、-C≡C-、Si(R ² ) ₂ 、C＝O、C＝S、C＝Se、C＝NR ² 、-C(＝O)O-、-C(＝O)NR ² -、NR ² 、P(＝O)(R ² ) -O-, -S-, SO or SO ₂ And wherein one or more hydrogen atoms may be replaced by D, F, cl, br, I, CN or NO ₂ Instead of, or as aromatic or heteroaromatic ring systems having from 5 to 60 aromatic ring atoms, each of which may be substituted by one or more R ² Substituted by radicals, or having 5 to 60 aromatic ring atoms and which may be substituted by one or more R ² Aryloxy or heteroaryloxy radical substituted by radicals, or having 5 to 60 aromatic ring atoms and which may be substituted by one or more R ² A group-substituted aralkyl or heteroaralkyl group, or a combination of these systems; simultaneously, two or more R ¹ The groups may together form a ring system; at the same time, one or more R ¹ A group may form a ring system with another part of the compound;

ar "is identical or different on each occurrence and is a substituted or unsubstituted aromatic ring having from 5 to 30 aromatic ring atoms and which may be substituted by one or more R ² A group-substituted aromatic or heteroaromatic ring system; at the same time, the two Ar' groups bonded to the same carbon, silicon, nitrogen, phosphorus or boron atom may also be linked via a bridging group by a single bond or be selected from B(R ² )、C(R ² ) ₂ 、Si(R ² ) ₂ 、C＝O、C＝NR ² 、C＝C(R ² ) ₂ 、O、S、S＝O、SO ₂ 、N(R ² )、P(R ² ) And P (= O) R ² Are linked together;

R ² identical or different on each occurrence and selected from H, D, F, CN, an aliphatic hydrocarbon radical having from 1 to 20 carbon atoms or an aromatic or heteroaromatic ring system having from 5 to 30 aromatic ring atoms in which one or more hydrogen atoms may be replaced by D, F, cl, br, I or CN and which may be substituted by one or more alkyl radicals each having from 1 to 4 carbon atoms; simultaneously, two or more substituents R ² May together form a ring system.

2. The compound of claim 1, comprising at least one structure of formulae (IIa) to (IIk),

wherein W ¹ 、W ² 、Y ¹ 、Y ² 、Z ¹ 、Z ² 、X ¹ 、X ² And X ³ Having the definitions given in claim 1, the further symbols and indices being as follows:

x is the same or different in each case and is N, CR, or if p is 1, X is C, provided that no more than two X groups in a ring are N;

Y ³ identical or different in each case and is O, S, N (Ar'), N (R), C = O, C (R) ₂ 、Si(R) ₂ 、C＝NR、C＝NAr'、C＝C(R) ₂ B (Ar'), or B (R);

p is 0 or 1.

3. The compound of claim 1 or 2, comprising at least one structure of formulae (IIIa) to (IIIk),

wherein Y is ¹ 、Y ² 、Z ¹ 、Z ² 、X ¹ 、X ² And X ³ Having the definition given in claim 1, the notation X, Y ³ And the subscript p has the definition given in claim 2.

4. The compound according to one or more of claims 1 to 3, comprising at least one structure of the formulae (IV-1) to (IV-20),

wherein Y is ¹ 、Y ² 、Z ¹ 、Z ² 、R、R ^a 、R ^b And R ^c Having the definition given in claim 1, the symbol Y ³ Having the definition given in claim 2, subscript l is 0, 1,2,3,4 or 5, subscript m is 0, 1,2,3 or 4, subscript n is 0, 1,2 or 3, subscript j is 0, 1 or 2, subscript k is 0 or 1.

5. Compound according to one or more of claims 1 to 4, characterized in that Z ¹ And Z ² At least one of the radicals is N, and Y ¹ And Y ² At least one of the groups is B (Ar), B (R), P (= O) Ar, P (= O) R, al (Ar), al (R), ga (Ar), ga (R), C = O, S = O or SO ₂ 。

6. Compound according to one or more of claims 1 to 5, characterized in that Z ¹ And Z ² At least one of the radicals is N, and Y ¹ And Y ² At least one of the groups is N (Ar), N (R), P (Ar), P (R), O, S, or Se.

7. Compound according to one or more of claims 1 to 6, characterized in that Z ¹ And Z ² At least one of the radicals is B, and Y ¹ And Y ² At least one of the groups is N (Ar), N (R), P (Ar), P (R), O, S or Se.

8. Compound according to one or more of claims 1 to 7, characterized in that Z ¹ And Z ² At least one of the radicals is B, and Y ¹ And Y ² At least one of the groups is B (Ar), B (R), P (= O) Ar, P (= O) R, al (Ar), al (R), ga (Ar), ga (R), C = O, S = O or SO ₂ 。

9. The compound according to one or more of claims 1 to 3 and 5 to 8, comprising at least one structure of formulae (V-1) to (V-40),

wherein Z ¹ 、Z ² 、X、X ¹ And X ² Having the definition given in claim 1, the symbol Y ³ Having the definition given in claim 2, Z ³ 、Z ⁴ In each caseIdentical or different and is N, B, P (= O) or Si (R).

10. The compound according to one or more of claims 1 to 9, comprising at least one structure of the formulae (VI-1) to (VI-40),

wherein the symbol Z ¹ 、Z ² 、R、R ^a And R ^b Having the definition given in claim 1, the symbol Y ³ Having the definition given in claim 2, Z ³ 、Z ⁴ Identical or different in each case and is N, B, P (= O) or Si (R), subscript l is 0, 1,2,3,4 or 5, subscript m is 0, 1,2,3 or 4, subscript j is 0, 1 or 2.

11. The device according to one or more of claims 1 to 10A compound characterized by at least two R, R ^a 、R ^b 、R ^c A group and a group of R, R ^a 、R ^b 、R ^c The additional groups to which the groups are attached together form a fused ring, wherein the two R, R ^a 、R ^b 、R ^c The groups forming at least one structure of formulae (RA-1) to (RA-12),

wherein R is ¹ Having the definition set forth above, the dashed bonds represent the two R, R of the group ^a 、R ^b 、R ^c The attachment site of the atom to which the group is bound, and the other symbols are defined as follows:

Y ⁴ in each case identical or different, and is C (R) ¹ ) ₂ 、(R ¹ ) ₂ C-C(R ¹ ) ₂ 、(R ¹ )C＝C(R ¹ )、NR ¹ NAr', O or S;

R ^d identical or different on each occurrence and is F, a linear alkyl, alkoxy or thioalkoxy group having from 1 to 40 carbon atoms or an alkenyl or alkynyl group having from 2 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having from 3 to 20 carbon atoms, where the alkyl, alkoxy, thioalkoxy, alkenyl or alkynyl group can in each case be substituted by one or more R ² Radical substitution of one or more non-adjacent CH ₂ The group can be represented by R ² C＝CR ² 、C≡C、Si(R ² ) ₂ 、C＝O、C＝S、C＝Se、C＝NR ² 、-C(＝O)O-、-C(＝O)NR ² -、NR ² 、P(＝O)(R ¹ ) -O-, -S-, SO or SO ₂ Instead of, or with 5 to 60 aromatic ring atoms andand may in each case be substituted by one or more R ² Aromatic or heteroaromatic ring systems substituted by radicals, or having 5 to 60 aromatic ring atoms and which may be substituted by one or more R ² A group-substituted aryloxy or heteroaryloxy group; at the same time, two R ^d The radicals together or one R ^d Group and R ¹ The radicals together or with further radicals may also form a ring system;

s is 0, 1,2,3,4, 5 or 6;

t is 0, 1,2,3,4, 5,6, 7 or 8;

v is 0, 1,2,3,4, 5,6, 7,8 or 9.

12. The compound of one or more of claims 1 to 11, wherein at least two R, R ^a 、R ^b 、R ^c A group and a group of R, R ^a 、R ^b 、R ^c The additional groups to which the groups are attached together form a fused ring, wherein the two R, R ^a 、R ^b 、R ^c The groups form the structure of formula (RB),

wherein R is ¹ Having the definition set forth in claim 1, the dashed bond representing the bond with said two R, R ^a 、R ^b 、R ^c The attachment site to which the group is attached, subscript m is 0, 1,2,3, or 4, and Y ⁵ Is C (R) ¹ ) ₂ 、NR ¹ 、NAr'、BR ¹ BAr', O or S.

13. The compound according to one or more of claims 1 to 12, comprising at least one structure of formulae (VII-1) to (VII-50), wherein the compound has at least one fused ring,

wherein Y is ¹ 、Y ² 、Z ¹ 、Z ² 、R、R ^a 、R ^b And R ^c Having the definition given in claim 1, the symbol Y ³ Having the definition given in claim 2, the symbol o denoting the attachment site, and the further symbols are defined as follows:

l is 0, 1,2,3,4 or 5;

m is 0, 1,2,3 or 4;

n is 0, 1,2 or 3;

j is 0, 1 or 2; and

k is 0 or 1.

14. An oligomer, polymer or dendrimer containing one or more compounds according to any one of claims 1 to 13, wherein one or more bonds of the compounds to the polymer, oligomer or dendrimer are present in place of a hydrogen atom or substituent.

15. A formulation comprising at least one compound according to one or more of claims 1 to 13 or an oligomer, polymer or dendrimer according to claim 14 and at least one further compound, wherein the further compound is preferably selected from one or more solvents.

16. A composition comprising at least one compound according to one or more of claims 1 to 13 or an oligomer, polymer or dendrimer according to claim 14 and at least one further compound selected from the group consisting of fluorescent emitters, phosphorescent emitters, emitters exhibiting TADF, host materials, electron-transporting materials, electron-injecting materials, hole-conducting materials, hole-injecting materials, electron-blocking materials and hole-blocking materials.

17. A process for the preparation of compounds according to one or more of claims 1 to 13, characterized in that the synthesis has Z ¹ Group or Z ² Group or Z ¹ 、Z ² A basic skeleton of a precursor of one of the groups, and Y is introduced by an aromatic nucleophilic substitution reaction or coupling reaction ¹ 、Y ² At least one of the groups.

18. Use of a compound according to one or more of claims 1 to 13 or an oligomer, polymer or dendrimer according to claim 14 in an electronic device.

19. An electronic device comprising at least one compound according to one or more of claims 1 to 13 or an oligomer, polymer or dendrimer according to claim 14.